Canonical Allele Identifier: CA357497639

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341829A>T (hg19) ; chr4:g.99420672A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420672A>T , CM000666.2:g.99420672A>T	GRCh38
NC_000004.11:g.100341829A>T , CM000666.1:g.100341829A>T	GRCh37
NC_000004.10:g.100560852A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.686T>A MANE Select	ENSP00000414254.2:p.Phe229Tyr
ENST00000209665.8:c.722T>A	ENSP00000209665.4:p.Phe241Tyr
ENST00000437033.6:c.686T>A	ENSP00000414254.2:p.Phe229Tyr
ENST00000476959.5:c.746T>A	ENSP00000420269.1:p.Phe249Tyr
ENST00000482593.5:c.515T>A	ENSP00000420613.1:p.Phe172Tyr
NM_000673.4:c.722T>A	NP_000664.2:p.Phe241Tyr
NM_001166504.1:c.746T>A	NP_001159976.1:p.Phe249Tyr
NM_000673.7:c.686T>A MANE Select	NP_000664.3:p.Phe229Tyr
NM_001166504.2:c.746T>A	NP_001159976.1:p.Phe249Tyr