Canonical Allele Identifier: CA440506426
Gene: ADH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100341810T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420653T>A , CM000666.2:g.99420653T>A GRCh38
NC_000004.11:g.100341810T>A , CM000666.1:g.100341810T>A GRCh37
NC_000004.10:g.100560833T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.705A>T MANE Select ENSP00000414254.2:p.Val235=
ENST00000209665.8:c.741A>T ENSP00000209665.4:p.Val247=
ENST00000437033.6:c.705A>T ENSP00000414254.2:p.Val235=
ENST00000476959.5:c.765A>T ENSP00000420269.1:p.Val255=
ENST00000482593.5:c.534A>T ENSP00000420613.1:p.Val178=
NM_000673.4:c.741A>T NP_000664.2:p.Val247=
NM_001166504.1:c.765A>T NP_001159976.1:p.Val255=
NM_000673.7:c.705A>T MANE Select NP_000664.3:p.Val235=
NM_001166504.2:c.765A>T NP_001159976.1:p.Val255=