Canonical Allele Identifier: CA357498618

Gene: ADH7

Linked Data

• COSMIC: COSM4584685 ; COSM4584686
• MyVariant Identifiers: chr4:g.100349679T>C (hg19) ; chr4:g.99428522T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99428522T>C , CM000666.2:g.99428522T>C	GRCh38
NC_000004.11:g.100349679T>C , CM000666.1:g.100349679T>C	GRCh37
NC_000004.10:g.100568702T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437033.7:c.229A>G MANE Select	ENSP00000414254.2:p.Ile77Val
ENST00000209665.8:c.265A>G	ENSP00000209665.4:p.Ile89Val
ENST00000437033.6:c.229A>G	ENSP00000414254.2:p.Ile77Val
ENST00000474027.1:c.58A>G	ENSP00000420300.1:p.Ile20Val
ENST00000476959.5:c.289A>G	ENSP00000420269.1:p.Ile97Val
ENST00000482593.5:c.58A>G	ENSP00000420613.1:p.Ile20Val
NM_000673.4:c.265A>G	NP_000664.2:p.Ile89Val
NM_001166504.1:c.289A>G	NP_001159976.1:p.Ile97Val
NM_000673.7:c.229A>G MANE Select	NP_000664.3:p.Ile77Val
NM_001166504.2:c.289A>G	NP_001159976.1:p.Ile97Val