ENST00000429967.3 APLN

Information
Transcript ID
ENST00000429967.3
Genome
hg38
Position
chrX:129,645,259-129,654,956
Strand
-
CDS length
234
Amino acid length
78
Gene symbol
APLN
Gene type
protein-coding
Gene description
apelin
Gene Entrez Gene ID
8862
Variants

Display target variant


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
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
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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 :
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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
Entry Origin Type Annotation
Exon
Exon number Start Stop
3 129,645,259 129,647,917
2 129,648,621 129,648,792
1 129,654,564 129,654,956
CDS
Exon number Type Start Stop
2 CDS 129,648,626 129,648,792
1 CDS 129,654,564 129,654,630
Other genome
Genome Chromosome Start End Links
hg19 chrX 128,779,236 128,788,933 Link
CDS sequence
ATGAATCTGCGGCTCTGCGTGCAGGCGCTCCTGCTGCTCTGGCTCTCCTTGACCGCGGTGTGTGGAGGGTCCCTGATGCCGCTTCCCGATGGGAATGGGCTGGAAGACGGCAATGTCCGCCACCTGGTGCAGCCCAGAGGGTCAAGGAATGGGCCAGGGCCCTGGCAGGGAGGTCGGAGGAAATTCCGCCGCCAGCGGCCCCGCCTCTCCCATAAGGGACCCATGCCTTTCTGA
Amino sequence
MNLRLCVQALLLLWLSLTAVCGGSLMPLPDGNGLEDGNVRHLVQPRGSRNGPGPWQGGRRKFRRQRPRLSHKGPMPF*