Canonical Allele Identifier: CA1479994339
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420699A= , CM000666.2:g.99420699A= GRCh38
NC_000004.11:g.100341856A= , CM000666.1:g.100341856A= GRCh37
NC_000004.10:g.100560879A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.659T= MANE Select ENSP00000414254.2:p.Ile220=
ENST00000209665.8:c.695T= ENSP00000209665.4:p.Ile232=
ENST00000437033.6:c.659T= ENSP00000414254.2:p.Ile220=
ENST00000476959.5:c.719T= ENSP00000420269.1:p.Ile240=
ENST00000482593.5:c.488T= ENSP00000420613.1:p.Ile163=
NM_000673.4:c.695T= NP_000664.2:p.Ile232=
NM_001166504.1:c.719T= NP_001159976.1:p.Ile240=
NM_000673.7:c.659T= MANE Select NP_000664.3:p.Ile220=
NM_001166504.2:c.719T= NP_001159976.1:p.Ile240=