Canonical Allele Identifier: CA1955197881

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553641A= , CM000673.2:g.17553641A=	GRCh38
NC_000011.9:g.17575188A= , CM000673.1:g.17575188A=	GRCh37
NC_000011.8:g.17531764A=	NCBI36
NG_033191.1:g.11269A=
NG_033191.2:g.11269A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.576+122A=	ENSP00000382323.2:n.576+122A=
ENST00000399397.6:c.540+122A= MANE Select	ENSP00000382329.2:n.540+122A=
ENST00000399391.6:c.576+122A=	ENSP00000382323.2:n.576+122A=
ENST00000399397.5:c.540+122A=	ENSP00000382329.2:n.540+122A=
ENST00000498332.5:n.446+122A=
NM_001277269.1:c.576+122A=	NP_001264198.1:n.576+122A=
NM_001292063.1:c.540+122A=	NP_001278992.1:n.540+122A=
NM_001277269.2:c.576+122A=	NP_001264198.1:n.576+122A=
NM_001292063.2:c.540+122A= MANE Select	NP_001278992.1:n.540+122A=