Canonical Allele Identifier: CA1955197658

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553232_17553233delinsAC , CM000673.2:g.17553232_17553233delinsAC	GRCh38
NC_000011.9:g.17574779_17574780delinsAC , CM000673.1:g.17574779_17574780delinsAC	GRCh37
NC_000011.8:g.17531355_17531356delinsAC	NCBI36
NG_033191.1:g.10860_10861delinsAC
NG_033191.2:g.10860_10861delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.421+21_421+22delinsAC	ENSP00000382323.2:n.421+21_421+22delinsAC
ENST00000399397.6:c.385+21_385+22delinsAC MANE Select	ENSP00000382329.2:n.385+21_385+22delinsAC
ENST00000399391.6:c.421+21_421+22delinsAC	ENSP00000382323.2:n.421+21_421+22delinsAC
ENST00000399397.5:c.385+21_385+22delinsAC	ENSP00000382329.2:n.385+21_385+22delinsAC
ENST00000428619.1:c.202+21_202+22delinsAC	ENSP00000399057.2:n.202+21_202+22delinsAC
ENST00000498332.5:n.291+21_291+22delinsAC
NM_001277269.1:c.421+21_421+22delinsAC	NP_001264198.1:n.421+21_421+22delinsAC
NM_001292063.1:c.385+21_385+22delinsAC	NP_001278992.1:n.385+21_385+22delinsAC
NM_001277269.2:c.421+21_421+22delinsAC	NP_001264198.1:n.421+21_421+22delinsAC
NM_001292063.2:c.385+21_385+22delinsAC MANE Select	NP_001278992.1:n.385+21_385+22delinsAC