Canonical Allele Identifier: CA2830555108

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553654_17553655insTG , CM000673.2:g.17553654_17553655insTG	GRCh38
NC_000011.9:g.17575201_17575202insTG , CM000673.1:g.17575201_17575202insTG	GRCh37
NC_000011.8:g.17531777_17531778insTG	NCBI36
NG_033191.1:g.11282_11283insTG
NG_033191.2:g.11282_11283insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.576+135_576+136insTG	ENSP00000382323.2:n.576+135_576+136insTG
ENST00000399397.6:c.540+135_540+136insTG MANE Select	ENSP00000382329.2:n.540+135_540+136insTG
ENST00000399391.6:c.576+135_576+136insTG	ENSP00000382323.2:n.576+135_576+136insTG
ENST00000399397.5:c.540+135_540+136insTG	ENSP00000382329.2:n.540+135_540+136insTG
ENST00000498332.5:n.446+135_446+136insTG
NM_001277269.1:c.576+135_576+136insTG	NP_001264198.1:n.576+135_576+136insTG
NM_001292063.1:c.540+135_540+136insTG	NP_001278992.1:n.540+135_540+136insTG
NM_001277269.2:c.576+135_576+136insTG	NP_001264198.1:n.576+135_576+136insTG
NM_001292063.2:c.540+135_540+136insTG MANE Select	NP_001278992.1:n.540+135_540+136insTG