Canonical Allele Identifier: CA357497875
Gene: ADH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420792A>T , CM000666.2:g.99420792A>T GRCh38
NC_000004.11:g.100341949A>T , CM000666.1:g.100341949A>T GRCh37
NC_000004.10:g.100560972A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.566T>A MANE Select ENSP00000414254.2:p.Val189Asp
ENST00000209665.8:c.602T>A ENSP00000209665.4:p.Val201Asp
ENST00000437033.6:c.566T>A ENSP00000414254.2:p.Val189Asp
ENST00000476959.5:c.626T>A ENSP00000420269.1:p.Val209Asp
ENST00000482593.5:c.395T>A ENSP00000420613.1:p.Val132Asp
NM_000673.4:c.602T>A NP_000664.2:p.Val201Asp
NM_001166504.1:c.626T>A NP_001159976.1:p.Val209Asp
NM_000673.7:c.566T>A MANE Select NP_000664.3:p.Val189Asp
NM_001166504.2:c.626T>A NP_001159976.1:p.Val209Asp