Canonical Allele Identifier: CA1479994739
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420971A= , CM000666.2:g.99420971A= GRCh38
NC_000004.11:g.100342128A= , CM000666.1:g.100342128A= GRCh37
NC_000004.10:g.100561151A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-178T= MANE Select ENSP00000414254.2:n.565-178T=
ENST00000209665.8:c.601-178T= ENSP00000209665.4:n.601-178T=
ENST00000437033.6:c.565-178T= ENSP00000414254.2:n.565-178T=
ENST00000476959.5:c.625-178T= ENSP00000420269.1:n.625-178T=
ENST00000482593.5:c.394-178T= ENSP00000420613.1:n.394-178T=
NM_000673.4:c.601-178T= NP_000664.2:n.601-178T=
NM_001166504.1:c.625-178T= NP_001159976.1:n.625-178T=
NM_000673.7:c.565-178T= MANE Select NP_000664.3:n.565-178T=
NM_001166504.2:c.625-178T= NP_001159976.1:n.625-178T=