Canonical Allele Identifier: CA440506450

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341863T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420706T>G , CM000666.2:g.99420706T>G	GRCh38
NC_000004.11:g.100341863T>G , CM000666.1:g.100341863T>G	GRCh37
NC_000004.10:g.100560886T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.652A>C MANE Select	ENSP00000414254.2:p.Arg218=
ENST00000209665.8:c.688A>C	ENSP00000209665.4:p.Arg230=
ENST00000437033.6:c.652A>C	ENSP00000414254.2:p.Arg218=
ENST00000476959.5:c.712A>C	ENSP00000420269.1:p.Arg238=
ENST00000482593.5:c.481A>C	ENSP00000420613.1:p.Arg161=
NM_000673.4:c.688A>C	NP_000664.2:p.Arg230=
NM_001166504.1:c.712A>C	NP_001159976.1:p.Arg238=
NM_000673.7:c.652A>C MANE Select	NP_000664.3:p.Arg218=
NM_001166504.2:c.712A>C	NP_001159976.1:p.Arg238=