Canonical Allele Identifier: CA440506387

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341750T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420593T>C , CM000666.2:g.99420593T>C	GRCh38
NC_000004.11:g.100341750T>C , CM000666.1:g.100341750T>C	GRCh37
NC_000004.10:g.100560773T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.765A>G MANE Select	ENSP00000414254.2:p.Ser255=
ENST00000209665.8:c.801A>G	ENSP00000209665.4:p.Ser267=
ENST00000437033.6:c.765A>G	ENSP00000414254.2:p.Ser255=
ENST00000476959.5:c.825A>G	ENSP00000420269.1:p.Ser275=
ENST00000482593.5:c.594A>G	ENSP00000420613.1:p.Ser198=
NM_000673.4:c.801A>G	NP_000664.2:p.Ser267=
NM_001166504.1:c.825A>G	NP_001159976.1:p.Ser275=
NM_000673.7:c.765A>G MANE Select	NP_000664.3:p.Ser255=
NM_001166504.2:c.825A>G	NP_001159976.1:p.Ser275=