Canonical Allele Identifier: CA1955237066

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635358C= , CM000673.2:g.17635358C=	GRCh38
NC_000011.9:g.17656905C= , CM000673.1:g.17656905C=	GRCh37
NC_000011.8:g.17613481C=	NCBI36
NG_033191.1:g.92986C=
NG_033191.2:g.92986C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+171C=	ENSP00000382323.2:n.7729+171C=
ENST00000399397.6:c.7693+171C= MANE Select	ENSP00000382329.2:n.7693+171C=
ENST00000342528.2:c.4322-252C=	ENSP00000341666.2:n.4322-252C=
ENST00000399391.6:c.7729+171C=	ENSP00000382323.2:n.7729+171C=
ENST00000399397.5:c.7693+171C=	ENSP00000382329.2:n.7693+171C=
NM_001277269.1:c.7729+171C=	NP_001264198.1:n.7729+171C=
NM_001292063.1:c.7693+171C=	NP_001278992.1:n.7693+171C=
NM_001277269.2:c.7729+171C=	NP_001264198.1:n.7729+171C=
NM_001292063.2:c.7693+171C= MANE Select	NP_001278992.1:n.7693+171C=