Canonical Allele Identifier: CA357497782

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341896C>A (hg19) ; chr4:g.99420739C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420739C>A , CM000666.2:g.99420739C>A	GRCh38
NC_000004.11:g.100341896C>A , CM000666.1:g.100341896C>A	GRCh37
NC_000004.10:g.100560919C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.619G>T MANE Select	ENSP00000414254.2:p.Val207Phe
ENST00000209665.8:c.655G>T	ENSP00000209665.4:p.Val219Phe
ENST00000437033.6:c.619G>T	ENSP00000414254.2:p.Val207Phe
ENST00000476959.5:c.679G>T	ENSP00000420269.1:p.Val227Phe
ENST00000482593.5:c.448G>T	ENSP00000420613.1:p.Val150Phe
NM_000673.4:c.655G>T	NP_000664.2:p.Val219Phe
NM_001166504.1:c.679G>T	NP_001159976.1:p.Val227Phe
NM_000673.7:c.619G>T MANE Select	NP_000664.3:p.Val207Phe
NM_001166504.2:c.679G>T	NP_001159976.1:p.Val227Phe