Canonical Allele Identifier: CA1955232969

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612457G= , CM000673.2:g.17612457G=	GRCh38
NC_000011.9:g.17634004G= , CM000673.1:g.17634004G=	GRCh37
NC_000011.8:g.17590580G=	NCBI36
NG_033191.1:g.70085G=
NG_033191.2:g.70085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6328+127G=	ENSP00000382323.2:n.6328+127G=
ENST00000399397.6:c.6292+127G= MANE Select	ENSP00000382329.2:n.6292+127G=
ENST00000342528.2:c.3346+127G=	ENSP00000341666.2:n.3346+127G=
ENST00000399391.6:c.6328+127G=	ENSP00000382323.2:n.6328+127G=
ENST00000399397.5:c.6292+127G=	ENSP00000382329.2:n.6292+127G=
NM_001277269.1:c.6328+127G=	NP_001264198.1:n.6328+127G=
NM_001292063.1:c.6292+127G=	NP_001278992.1:n.6292+127G=
NM_001277269.2:c.6328+127G=	NP_001264198.1:n.6328+127G=
NM_001292063.2:c.6292+127G= MANE Select	NP_001278992.1:n.6292+127G=