ALLC allantoicase

Information
Symbol
ALLC
Type
protein-coding
Description
allantoicase
Entrez Gene ID
55821
Genome
hg19
Position
chr2:3,705,790-3,750,261
Genome
hg38
Position
chr2:3,658,200-3,702,671
MIM
612396 OMIM
HGNC
HGNC:17377 HGNC
Ensembl
ENSG00000151360 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 1 0
Benign 0 4
Likely benign 0 4
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
56
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM ALC
MIM 612396 OMIM
HGNC HGNC:17377 HGNC
Ensembl ENSG00000151360 Ensembl
AllianceGenome HGNC:17377
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000252505.4 hg38 chr2 3,658,200 3,702,671 44,472
ENST00000252505.4 hg19 chr2 3,705,790 3,750,261 44,472
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