Canonical Allele Identifier: CA1955233167

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612850_17612851delinsCA , CM000673.2:g.17612850_17612851delinsCA	GRCh38
NC_000011.9:g.17634397_17634398delinsCA , CM000673.1:g.17634397_17634398delinsCA	GRCh37
NC_000011.8:g.17590973_17590974delinsCA	NCBI36
NG_033191.1:g.70478_70479delinsCA
NG_033191.2:g.70478_70479delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6474+85_6474+86delinsCA	ENSP00000382323.2:n.6474+85_6474+86delinsCA
ENST00000399397.6:c.6438+85_6438+86delinsCA MANE Select	ENSP00000382329.2:n.6438+85_6438+86delinsCA
ENST00000342528.2:c.3492+85_3492+86delinsCA	ENSP00000341666.2:n.3492+85_3492+86delinsCA
ENST00000399391.6:c.6474+85_6474+86delinsCA	ENSP00000382323.2:n.6474+85_6474+86delinsCA
ENST00000399397.5:c.6438+85_6438+86delinsCA	ENSP00000382329.2:n.6438+85_6438+86delinsCA
NM_001277269.1:c.6474+85_6474+86delinsCA	NP_001264198.1:n.6474+85_6474+86delinsCA
NM_001292063.1:c.6438+85_6438+86delinsCA	NP_001278992.1:n.6438+85_6438+86delinsCA
NM_001277269.2:c.6474+85_6474+86delinsCA	NP_001264198.1:n.6474+85_6474+86delinsCA
NM_001292063.2:c.6438+85_6438+86delinsCA MANE Select	NP_001278992.1:n.6438+85_6438+86delinsCA