Canonical Allele Identifier: CA1480005180
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428427A= , CM000666.2:g.99428427A= GRCh38
NC_000004.11:g.100349584A= , CM000666.1:g.100349584A= GRCh37
NC_000004.10:g.100568607A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437033.7:c.259+65T= MANE Select ENSP00000414254.2:n.259+65T=
ENST00000209665.8:c.295+65T= ENSP00000209665.4:n.295+65T=
ENST00000437033.6:c.259+65T= ENSP00000414254.2:n.259+65T=
ENST00000474027.1:c.88+65T= ENSP00000420300.1:n.88+65T=
ENST00000476959.5:c.319+65T= ENSP00000420269.1:n.319+65T=
ENST00000482593.5:c.88+65T= ENSP00000420613.1:n.88+65T=
NM_000673.4:c.295+65T= NP_000664.2:n.295+65T=
NM_001166504.1:c.319+65T= NP_001159976.1:n.319+65T=
NM_000673.7:c.259+65T= MANE Select NP_000664.3:n.259+65T=
NM_001166504.2:c.319+65T= NP_001159976.1:n.319+65T=