Canonical Allele Identifier: CA102645891

Gene: ADH7

Linked Data

• dbSNP Id: rs375067624
• COSMIC: COSM5580156 ; COSM5580157
• MyVariant Identifiers: chr4:g.100341783C>T (hg19) ; chr4:g.99420626C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420626C>T , CM000666.2:g.99420626C>T	GRCh38
NC_000004.11:g.100341783C>T , CM000666.1:g.100341783C>T	GRCh37
NC_000004.10:g.100560806C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.732G>A MANE Select	ENSP00000414254.2:p.Lys244=
ENST00000209665.8:c.768G>A	ENSP00000209665.4:p.Lys256=
ENST00000437033.6:c.732G>A	ENSP00000414254.2:p.Lys244=
ENST00000476959.5:c.792G>A	ENSP00000420269.1:p.Lys264=
ENST00000482593.5:c.561G>A	ENSP00000420613.1:p.Lys187=
NM_000673.4:c.768G>A	NP_000664.2:p.Lys256=
NM_001166504.1:c.792G>A	NP_001159976.1:p.Lys264=
NM_000673.7:c.732G>A MANE Select	NP_000664.3:p.Lys244=
NM_001166504.2:c.792G>A	NP_001159976.1:p.Lys264=