Canonical Allele Identifier: CA357497461

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341744C>G (hg19) ; chr4:g.99420587C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420587C>G , CM000666.2:g.99420587C>G	GRCh38
NC_000004.11:g.100341744C>G , CM000666.1:g.100341744C>G	GRCh37
NC_000004.10:g.100560767C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.771G>C MANE Select	ENSP00000414254.2:p.Met257Ile
ENST00000209665.8:c.807G>C	ENSP00000209665.4:p.Met269Ile
ENST00000437033.6:c.771G>C	ENSP00000414254.2:p.Met257Ile
ENST00000476959.5:c.831G>C	ENSP00000420269.1:p.Met277Ile
ENST00000482593.5:c.600G>C	ENSP00000420613.1:p.Met200Ile
NM_000673.4:c.807G>C	NP_000664.2:p.Met269Ile
NM_001166504.1:c.831G>C	NP_001159976.1:p.Met277Ile
NM_000673.7:c.771G>C MANE Select	NP_000664.3:p.Met257Ile
NM_001166504.2:c.831G>C	NP_001159976.1:p.Met277Ile