Canonical Allele Identifier: CA1479994261
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420673A= , CM000666.2:g.99420673A= GRCh38
NC_000004.11:g.100341830A= , CM000666.1:g.100341830A= GRCh37
NC_000004.10:g.100560853A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.685T= MANE Select ENSP00000414254.2:p.Phe229=
ENST00000209665.8:c.721T= ENSP00000209665.4:p.Phe241=
ENST00000437033.6:c.685T= ENSP00000414254.2:p.Phe229=
ENST00000476959.5:c.745T= ENSP00000420269.1:p.Phe249=
ENST00000482593.5:c.514T= ENSP00000420613.1:p.Phe172=
NM_000673.4:c.721T= NP_000664.2:p.Phe241=
NM_001166504.1:c.745T= NP_001159976.1:p.Phe249=
NM_000673.7:c.685T= MANE Select NP_000664.3:p.Phe229=
NM_001166504.2:c.745T= NP_001159976.1:p.Phe249=