Canonical Allele Identifier: CA357497391

Gene: ADH7

Linked Data

• gnomAD v4: 4-99420555-A-T
• MyVariant Identifiers: chr4:g.100341712A>T (hg19) ; chr4:g.99420555A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.803T>A MANE Select	ENSP00000414254.2:p.Val268Asp
ENST00000209665.8:c.839T>A	ENSP00000209665.4:p.Val280Asp
ENST00000437033.6:c.803T>A	ENSP00000414254.2:p.Val268Asp
ENST00000476959.5:c.863T>A	ENSP00000420269.1:p.Val288Asp
ENST00000482593.5:c.632T>A	ENSP00000420613.1:p.Val211Asp
NM_000673.4:c.839T>A	NP_000664.2:p.Val280Asp
NM_001166504.1:c.863T>A	NP_001159976.1:p.Val288Asp
NM_000673.7:c.803T>A MANE Select	NP_000664.3:p.Val268Asp
NM_001166504.2:c.863T>A	NP_001159976.1:p.Val288Asp