Canonical Allele Identifier: CA357497655

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341835T>G (hg19) ; chr4:g.99420678T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420678T>G , CM000666.2:g.99420678T>G	GRCh38
NC_000004.11:g.100341835T>G , CM000666.1:g.100341835T>G	GRCh37
NC_000004.10:g.100560858T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.680A>C MANE Select	ENSP00000414254.2:p.Asp227Ala
ENST00000209665.8:c.716A>C	ENSP00000209665.4:p.Asp239Ala
ENST00000437033.6:c.680A>C	ENSP00000414254.2:p.Asp227Ala
ENST00000476959.5:c.740A>C	ENSP00000420269.1:p.Asp247Ala
ENST00000482593.5:c.509A>C	ENSP00000420613.1:p.Asp170Ala
NM_000673.4:c.716A>C	NP_000664.2:p.Asp239Ala
NM_001166504.1:c.740A>C	NP_001159976.1:p.Asp247Ala
NM_000673.7:c.680A>C MANE Select	NP_000664.3:p.Asp227Ala
NM_001166504.2:c.740A>C	NP_001159976.1:p.Asp247Ala