Canonical Allele Identifier: CA357497355

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341695T>G (hg19) ; chr4:g.99420538T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420538T>G , CM000666.2:g.99420538T>G	GRCh38
NC_000004.11:g.100341695T>G , CM000666.1:g.100341695T>G	GRCh37
NC_000004.10:g.100560718T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.820A>C MANE Select	ENSP00000414254.2:p.Thr274Pro
ENST00000209665.8:c.856A>C	ENSP00000209665.4:p.Thr286Pro
ENST00000437033.6:c.820A>C	ENSP00000414254.2:p.Thr274Pro
ENST00000476959.5:c.880A>C	ENSP00000420269.1:p.Thr294Pro
ENST00000482593.5:c.649A>C	ENSP00000420613.1:p.Thr217Pro
NM_000673.4:c.856A>C	NP_000664.2:p.Thr286Pro
NM_001166504.1:c.880A>C	NP_001159976.1:p.Thr294Pro
NM_000673.7:c.820A>C MANE Select	NP_000664.3:p.Thr274Pro
NM_001166504.2:c.880A>C	NP_001159976.1:p.Thr294Pro