Canonical Allele Identifier: CA1480005376
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428591T= , CM000666.2:g.99428591T= GRCh38
NC_000004.11:g.100349748T= , CM000666.1:g.100349748T= GRCh37
NC_000004.10:g.100568771T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.160A= MANE Select ENSP00000414254.2:p.Ile54=
ENST00000209665.8:c.196A= ENSP00000209665.4:p.Ile66=
ENST00000437033.6:c.160A= ENSP00000414254.2:p.Ile54=
ENST00000474027.1:c.-12A= ENSP00000420300.1:n.-12A=
ENST00000476959.5:c.220A= ENSP00000420269.1:p.Ile74=
ENST00000482593.5:c.-12A= ENSP00000420613.1:n.-12A=
NM_000673.4:c.196A= NP_000664.2:p.Ile66=
NM_001166504.1:c.220A= NP_001159976.1:p.Ile74=
NM_000673.7:c.160A= MANE Select NP_000664.3:p.Ile54=
NM_001166504.2:c.220A= NP_001159976.1:p.Ile74=