Canonical Allele Identifier: CA1955232921

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612378_17612380delinsACC , CM000673.2:g.17612378_17612380delinsACC	GRCh38
NC_000011.9:g.17633925_17633927delinsACC , CM000673.1:g.17633925_17633927delinsACC	GRCh37
NC_000011.8:g.17590501_17590503delinsACC	NCBI36
NG_033191.1:g.70006_70008delinsACC
NG_033191.2:g.70006_70008delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6328+48_6328+50delinsACC	ENSP00000382323.2:n.6328+48_6328+50delinsACC
ENST00000399397.6:c.6292+48_6292+50delinsACC MANE Select	ENSP00000382329.2:n.6292+48_6292+50delinsACC
ENST00000342528.2:c.3346+48_3346+50delinsACC	ENSP00000341666.2:n.3346+48_3346+50delinsACC
ENST00000399391.6:c.6328+48_6328+50delinsACC	ENSP00000382323.2:n.6328+48_6328+50delinsACC
ENST00000399397.5:c.6292+48_6292+50delinsACC	ENSP00000382329.2:n.6292+48_6292+50delinsACC
NM_001277269.1:c.6328+48_6328+50delinsACC	NP_001264198.1:n.6328+48_6328+50delinsACC
NM_001292063.1:c.6292+48_6292+50delinsACC	NP_001278992.1:n.6292+48_6292+50delinsACC
NM_001277269.2:c.6328+48_6328+50delinsACC	NP_001264198.1:n.6328+48_6328+50delinsACC
NM_001292063.2:c.6292+48_6292+50delinsACC MANE Select	NP_001278992.1:n.6292+48_6292+50delinsACC