Canonical Allele Identifier: CA1479994027
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420564G= , CM000666.2:g.99420564G= GRCh38
NC_000004.11:g.100341721G= , CM000666.1:g.100341721G= GRCh37
NC_000004.10:g.100560744G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.794C= MANE Select ENSP00000414254.2:p.Thr265=
ENST00000209665.8:c.830C= ENSP00000209665.4:p.Thr277=
ENST00000437033.6:c.794C= ENSP00000414254.2:p.Thr265=
ENST00000476959.5:c.854C= ENSP00000420269.1:p.Thr285=
ENST00000482593.5:c.623C= ENSP00000420613.1:p.Thr208=
NM_000673.4:c.830C= NP_000664.2:p.Thr277=
NM_001166504.1:c.854C= NP_001159976.1:p.Thr285=
NM_000673.7:c.794C= MANE Select NP_000664.3:p.Thr265=
NM_001166504.2:c.854C= NP_001159976.1:p.Thr285=