Canonical Allele Identifier: CA1955233090
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612706A= , CM000673.2:g.17612706A= GRCh38
NC_000011.9:g.17634253A= , CM000673.1:g.17634253A= GRCh37
NC_000011.8:g.17590829A= NCBI36
NG_033191.1:g.70334A=
NG_033191.2:g.70334A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6415A= ENSP00000382323.2:p.Ser2139=
ENST00000399397.6:c.6379A= MANE Select ENSP00000382329.2:p.Ser2127=
ENST00000342528.2:c.3433A= ENSP00000341666.2:p.Ser1145=
ENST00000399391.6:c.6415A= ENSP00000382323.2:p.Ser2139=
ENST00000399397.5:c.6379A= ENSP00000382329.2:p.Ser2127=
NM_001277269.1:c.6415A= NP_001264198.1:p.Ser2139=
NM_001292063.1:c.6379A= NP_001278992.1:p.Ser2127=
NM_001277269.2:c.6415A= NP_001264198.1:p.Ser2139=
NM_001292063.2:c.6379A= MANE Select NP_001278992.1:p.Ser2127=