Canonical Allele Identifier: CA440506413

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341789A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420632A>G , CM000666.2:g.99420632A>G	GRCh38
NC_000004.11:g.100341789A>G , CM000666.1:g.100341789A>G	GRCh37
NC_000004.10:g.100560812A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.726T>C MANE Select	ENSP00000414254.2:p.Ser242=
ENST00000209665.8:c.762T>C	ENSP00000209665.4:p.Ser254=
ENST00000437033.6:c.726T>C	ENSP00000414254.2:p.Ser242=
ENST00000476959.5:c.786T>C	ENSP00000420269.1:p.Ser262=
ENST00000482593.5:c.555T>C	ENSP00000420613.1:p.Ser185=
NM_000673.4:c.762T>C	NP_000664.2:p.Ser254=
NM_001166504.1:c.786T>C	NP_001159976.1:p.Ser262=
NM_000673.7:c.726T>C MANE Select	NP_000664.3:p.Ser242=
NM_001166504.2:c.786T>C	NP_001159976.1:p.Ser262=