Canonical Allele Identifier: CA357497861

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341941C>T (hg19) ; chr4:g.99420784C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420784C>T , CM000666.2:g.99420784C>T	GRCh38
NC_000004.11:g.100341941C>T , CM000666.1:g.100341941C>T	GRCh37
NC_000004.10:g.100560964C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.574G>A MANE Select	ENSP00000414254.2:p.Gly192Ser
ENST00000209665.8:c.610G>A	ENSP00000209665.4:p.Gly204Ser
ENST00000437033.6:c.574G>A	ENSP00000414254.2:p.Gly192Ser
ENST00000476959.5:c.634G>A	ENSP00000420269.1:p.Gly212Ser
ENST00000482593.5:c.403G>A	ENSP00000420613.1:p.Gly135Ser
NM_000673.4:c.610G>A	NP_000664.2:p.Gly204Ser
NM_001166504.1:c.634G>A	NP_001159976.1:p.Gly212Ser
NM_000673.7:c.574G>A MANE Select	NP_000664.3:p.Gly192Ser
NM_001166504.2:c.634G>A	NP_001159976.1:p.Gly212Ser