Canonical Allele Identifier: CA440318645

Gene: ADH7

Linked Data

• dbSNP Id: rs1341899704
• MyVariant Identifiers: chr4:g.100349677A>G (hg19) ; chr4:g.99428520A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99428520A>G , CM000666.2:g.99428520A>G	GRCh38
NC_000004.11:g.100349677A>G , CM000666.1:g.100349677A>G	GRCh37
NC_000004.10:g.100568700A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437033.7:c.231T>C MANE Select	ENSP00000414254.2:p.Ile77=
ENST00000209665.8:c.267T>C	ENSP00000209665.4:p.Ile89=
ENST00000437033.6:c.231T>C	ENSP00000414254.2:p.Ile77=
ENST00000474027.1:c.60T>C	ENSP00000420300.1:p.Ile20=
ENST00000476959.5:c.291T>C	ENSP00000420269.1:p.Ile97=
ENST00000482593.5:c.60T>C	ENSP00000420613.1:p.Ile20=
NM_000673.4:c.267T>C	NP_000664.2:p.Ile89=
NM_001166504.1:c.291T>C	NP_001159976.1:p.Ile97=
NM_000673.7:c.231T>C MANE Select	NP_000664.3:p.Ile77=
NM_001166504.2:c.291T>C	NP_001159976.1:p.Ile97=