Canonical Allele Identifier: CA1480005280
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428521A= , CM000666.2:g.99428521A= GRCh38
NC_000004.11:g.100349678A= , CM000666.1:g.100349678A= GRCh37
NC_000004.10:g.100568701A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437033.7:c.230T= MANE Select ENSP00000414254.2:p.Ile77=
ENST00000209665.8:c.266T= ENSP00000209665.4:p.Ile89=
ENST00000437033.6:c.230T= ENSP00000414254.2:p.Ile77=
ENST00000474027.1:c.59T= ENSP00000420300.1:p.Ile20=
ENST00000476959.5:c.290T= ENSP00000420269.1:p.Ile97=
ENST00000482593.5:c.59T= ENSP00000420613.1:p.Ile20=
NM_000673.4:c.266T= NP_000664.2:p.Ile89=
NM_001166504.1:c.290T= NP_001159976.1:p.Ile97=
NM_000673.7:c.230T= MANE Select NP_000664.3:p.Ile77=
NM_001166504.2:c.290T= NP_001159976.1:p.Ile97=