Canonical Allele Identifier: CA1955233069

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612664G= , CM000673.2:g.17612664G=	GRCh38
NC_000011.9:g.17634211G= , CM000673.1:g.17634211G=	GRCh37
NC_000011.8:g.17590787G=	NCBI36
NG_033191.1:g.70292G=
NG_033191.2:g.70292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6373G=	ENSP00000382323.2:p.Gly2125=
ENST00000399397.6:c.6337G= MANE Select	ENSP00000382329.2:p.Gly2113=
ENST00000342528.2:c.3391G=	ENSP00000341666.2:p.Gly1131=
ENST00000399391.6:c.6373G=	ENSP00000382323.2:p.Gly2125=
ENST00000399397.5:c.6337G=	ENSP00000382329.2:p.Gly2113=
NM_001277269.1:c.6373G=	NP_001264198.1:p.Gly2125=
NM_001292063.1:c.6337G=	NP_001278992.1:p.Gly2113=
NM_001277269.2:c.6373G=	NP_001264198.1:p.Gly2125=
NM_001292063.2:c.6337G= MANE Select	NP_001278992.1:p.Gly2113=