HOXA11-AS HOXA11 antisense RNA
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | HOXA-AS5 |
SYNONYM | HOXA11-AS1 |
SYNONYM | HOXA11AS |
SYNONYM | HOXA11S |
SYNONYM | LncHOXA11 |
SYNONYM | NCRNA00076 |
MIM | 607530 OMIM |
HGNC | HGNC:24957 HGNC |
Ensembl | ENSG00000240990 Ensembl |
AllianceGenome | HGNC:24957 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000522674.1 | hg38 | chr7 | 27,185,408 | 27,189,293 | 3,886 |
ENST00000650141.1 | hg38 | chr7 | 27,186,134 | 27,189,083 | 2,950 |
ENST00000648491.1 | hg38 | chr7 | 27,185,423 | 27,189,298 | 3,876 |
ENST00000522863.2 | hg38 | chr7 | 27,184,671 | 27,189,169 | 4,499 |
ENST00000522863.2 | hg19 | chr7 | 27,224,290 | 27,228,788 | 4,499 |
ENST00000522674.1 | hg19 | chr7 | 27,225,027 | 27,228,912 | 3,886 |
ENST00000648491.1 | hg19 | chr7 | 27,225,042 | 27,228,917 | 3,876 |
ENST00000650141.1 | hg19 | chr7 | 27,225,753 | 27,228,702 | 2,950 |
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