Canonical Allele Identifier: CA1479993476
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420260A= , CM000666.2:g.99420260A= GRCh38
NC_000004.11:g.100341417A= , CM000666.1:g.100341417A= GRCh37
NC_000004.10:g.100560440A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+273T= MANE Select ENSP00000414254.2:n.825+273T=
ENST00000209665.8:c.861+273T= ENSP00000209665.4:n.861+273T=
ENST00000437033.6:c.825+273T= ENSP00000414254.2:n.825+273T=
ENST00000476959.5:c.885+273T= ENSP00000420269.1:n.885+273T=
ENST00000482593.5:c.654+273T= ENSP00000420613.1:n.654+273T=
NM_000673.4:c.861+273T= NP_000664.2:n.861+273T=
NM_001166504.1:c.885+273T= NP_001159976.1:n.885+273T=
NM_000673.7:c.825+273T= MANE Select NP_000664.3:n.825+273T=
NM_001166504.2:c.885+273T= NP_001159976.1:n.885+273T=