Canonical Allele Identifier: CA357498782

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100349756T>C (hg19) ; chr4:g.99428599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99428599T>C , CM000666.2:g.99428599T>C	GRCh38
NC_000004.11:g.100349756T>C , CM000666.1:g.100349756T>C	GRCh37
NC_000004.10:g.100568779T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.152A>G MANE Select	ENSP00000414254.2:p.Asp51Gly
ENST00000209665.8:c.188A>G	ENSP00000209665.4:p.Asp63Gly
ENST00000437033.6:c.152A>G	ENSP00000414254.2:p.Asp51Gly
ENST00000474027.1:c.-20A>G	ENSP00000420300.1:n.-20A>G
ENST00000476959.5:c.212A>G	ENSP00000420269.1:p.Asp71Gly
ENST00000482593.5:c.-20A>G	ENSP00000420613.1:n.-20A>G
NM_000673.4:c.188A>G	NP_000664.2:p.Asp63Gly
NM_001166504.1:c.212A>G	NP_001159976.1:p.Asp71Gly
NM_000673.7:c.152A>G MANE Select	NP_000664.3:p.Asp51Gly
NM_001166504.2:c.212A>G	NP_001159976.1:p.Asp71Gly