Canonical Allele Identifier: CA357497863

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341943G>C (hg19) ; chr4:g.99420786G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420786G>C , CM000666.2:g.99420786G>C	GRCh38
NC_000004.11:g.100341943G>C , CM000666.1:g.100341943G>C	GRCh37
NC_000004.10:g.100560966G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.572C>G MANE Select	ENSP00000414254.2:p.Pro191Arg
ENST00000209665.8:c.608C>G	ENSP00000209665.4:p.Pro203Arg
ENST00000437033.6:c.572C>G	ENSP00000414254.2:p.Pro191Arg
ENST00000476959.5:c.632C>G	ENSP00000420269.1:p.Pro211Arg
ENST00000482593.5:c.401C>G	ENSP00000420613.1:p.Pro134Arg
NM_000673.4:c.608C>G	NP_000664.2:p.Pro203Arg
NM_001166504.1:c.632C>G	NP_001159976.1:p.Pro211Arg
NM_000673.7:c.572C>G MANE Select	NP_000664.3:p.Pro191Arg
NM_001166504.2:c.632C>G	NP_001159976.1:p.Pro211Arg