Canonical Allele Identifier: CA1479994075
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420585G= , CM000666.2:g.99420585G= GRCh38
NC_000004.11:g.100341742G= , CM000666.1:g.100341742G= GRCh37
NC_000004.10:g.100560765G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.773C= MANE Select ENSP00000414254.2:p.Thr258=
ENST00000209665.8:c.809C= ENSP00000209665.4:p.Thr270=
ENST00000437033.6:c.773C= ENSP00000414254.2:p.Thr258=
ENST00000476959.5:c.833C= ENSP00000420269.1:p.Thr278=
ENST00000482593.5:c.602C= ENSP00000420613.1:p.Thr201=
NM_000673.4:c.809C= NP_000664.2:p.Thr270=
NM_001166504.1:c.833C= NP_001159976.1:p.Thr278=
NM_000673.7:c.773C= MANE Select NP_000664.3:p.Thr258=
NM_001166504.2:c.833C= NP_001159976.1:p.Thr278=