Canonical Allele Identifier: CA357498602

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100349672T>A (hg19) ; chr4:g.99428515T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99428515T>A , CM000666.2:g.99428515T>A	GRCh38
NC_000004.11:g.100349672T>A , CM000666.1:g.100349672T>A	GRCh37
NC_000004.10:g.100568695T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437033.7:c.236A>T MANE Select	ENSP00000414254.2:p.Glu79Val
ENST00000209665.8:c.272A>T	ENSP00000209665.4:p.Glu91Val
ENST00000437033.6:c.236A>T	ENSP00000414254.2:p.Glu79Val
ENST00000474027.1:c.65A>T	ENSP00000420300.1:p.Glu22Val
ENST00000476959.5:c.296A>T	ENSP00000420269.1:p.Glu99Val
ENST00000482593.5:c.65A>T	ENSP00000420613.1:p.Glu22Val
NM_000673.4:c.272A>T	NP_000664.2:p.Glu91Val
NM_001166504.1:c.296A>T	NP_001159976.1:p.Glu99Val
NM_000673.7:c.236A>T MANE Select	NP_000664.3:p.Glu79Val
NM_001166504.2:c.296A>T	NP_001159976.1:p.Glu99Val