Canonical Allele Identifier: CA440506376

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341729C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420572C>G , CM000666.2:g.99420572C>G	GRCh38
NC_000004.11:g.100341729C>G , CM000666.1:g.100341729C>G	GRCh37
NC_000004.10:g.100560752C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.786G>C MANE Select	ENSP00000414254.2:p.Val262=
ENST00000209665.8:c.822G>C	ENSP00000209665.4:p.Val274=
ENST00000437033.6:c.786G>C	ENSP00000414254.2:p.Val262=
ENST00000476959.5:c.846G>C	ENSP00000420269.1:p.Val282=
ENST00000482593.5:c.615G>C	ENSP00000420613.1:p.Val205=
NM_000673.4:c.822G>C	NP_000664.2:p.Val274=
NM_001166504.1:c.846G>C	NP_001159976.1:p.Val282=
NM_000673.7:c.786G>C MANE Select	NP_000664.3:p.Val262=
NM_001166504.2:c.846G>C	NP_001159976.1:p.Val282=