Canonical Allele Identifier: CA1479994697
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420938T= , CM000666.2:g.99420938T= GRCh38
NC_000004.11:g.100342095T= , CM000666.1:g.100342095T= GRCh37
NC_000004.10:g.100561118T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-145A= MANE Select ENSP00000414254.2:n.565-145A=
ENST00000209665.8:c.601-145A= ENSP00000209665.4:n.601-145A=
ENST00000437033.6:c.565-145A= ENSP00000414254.2:n.565-145A=
ENST00000476959.5:c.625-145A= ENSP00000420269.1:n.625-145A=
ENST00000482593.5:c.394-145A= ENSP00000420613.1:n.394-145A=
NM_000673.4:c.601-145A= NP_000664.2:n.601-145A=
NM_001166504.1:c.625-145A= NP_001159976.1:n.625-145A=
NM_000673.7:c.565-145A= MANE Select NP_000664.3:n.565-145A=
NM_001166504.2:c.625-145A= NP_001159976.1:n.625-145A=