Canonical Allele Identifier: CA357497389
Gene: ADH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420555A>C , CM000666.2:g.99420555A>C GRCh38
NC_000004.11:g.100341712A>C , CM000666.1:g.100341712A>C GRCh37
NC_000004.10:g.100560735A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.803T>G MANE Select ENSP00000414254.2:p.Val268Gly
ENST00000209665.8:c.839T>G ENSP00000209665.4:p.Val280Gly
ENST00000437033.6:c.803T>G ENSP00000414254.2:p.Val268Gly
ENST00000476959.5:c.863T>G ENSP00000420269.1:p.Val288Gly
ENST00000482593.5:c.632T>G ENSP00000420613.1:p.Val211Gly
NM_000673.4:c.839T>G NP_000664.2:p.Val280Gly
NM_001166504.1:c.863T>G NP_001159976.1:p.Val288Gly
NM_000673.7:c.803T>G MANE Select NP_000664.3:p.Val268Gly
NM_001166504.2:c.863T>G NP_001159976.1:p.Val288Gly