Canonical Allele Identifier: CA1955236804
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17634878C= , CM000673.2:g.17634878C= GRCh38
NC_000011.9:g.17656425C= , CM000673.1:g.17656425C= GRCh37
NC_000011.8:g.17613001C= NCBI36
NG_033191.1:g.92506C=
NG_033191.2:g.92506C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7551C= ENSP00000382323.2:p.Pro2517=
ENST00000399397.6:c.7515C= MANE Select ENSP00000382329.2:p.Pro2505=
ENST00000342528.2:c.4322-732C= ENSP00000341666.2:n.4322-732C=
ENST00000399391.6:c.7551C= ENSP00000382323.2:p.Pro2517=
ENST00000399397.5:c.7515C= ENSP00000382329.2:p.Pro2505=
NM_001277269.1:c.7551C= NP_001264198.1:p.Pro2517=
NM_001292063.1:c.7515C= NP_001278992.1:p.Pro2505=
NM_001277269.2:c.7551C= NP_001264198.1:p.Pro2517=
NM_001292063.2:c.7515C= MANE Select NP_001278992.1:p.Pro2505=