Canonical Allele Identifier: CA1955217100
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17594037C= , CM000673.2:g.17594037C= GRCh38
NC_000011.9:g.17615584C= , CM000673.1:g.17615584C= GRCh37
NC_000011.8:g.17572160C= NCBI36
NG_033191.1:g.51665C=
NG_033191.2:g.51665C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.3325-10C= ENSP00000382323.2:n.3325-10C=
ENST00000399397.6:c.3289-10C= MANE Select ENSP00000382329.2:n.3289-10C=
ENST00000342528.2:c.370-10C= ENSP00000341666.2:n.370-10C=
ENST00000399391.6:c.3325-10C= ENSP00000382323.2:n.3325-10C=
ENST00000399397.5:c.3289-10C= ENSP00000382329.2:n.3289-10C=
NM_001277269.1:c.3325-10C= NP_001264198.1:n.3325-10C=
NM_001292063.1:c.3289-10C= NP_001278992.1:n.3289-10C=
NM_001277269.2:c.3325-10C= NP_001264198.1:n.3325-10C=
NM_001292063.2:c.3289-10C= MANE Select NP_001278992.1:n.3289-10C=