Canonical Allele Identifier: CA1955236972

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635176C= , CM000673.2:g.17635176C=	GRCh38
NC_000011.9:g.17656723C= , CM000673.1:g.17656723C=	GRCh37
NC_000011.8:g.17613299C=	NCBI36
NG_033191.1:g.92804C=
NG_033191.2:g.92804C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7718C=	ENSP00000382323.2:p.Ser2573=
ENST00000399397.6:c.7682C= MANE Select	ENSP00000382329.2:p.Ser2561=
ENST00000342528.2:c.4322-434C=	ENSP00000341666.2:n.4322-434C=
ENST00000399391.6:c.7718C=	ENSP00000382323.2:p.Ser2573=
ENST00000399397.5:c.7682C=	ENSP00000382329.2:p.Ser2561=
NM_001277269.1:c.7718C=	NP_001264198.1:p.Ser2573=
NM_001292063.1:c.7682C=	NP_001278992.1:p.Ser2561=
NM_001277269.2:c.7718C=	NP_001264198.1:p.Ser2573=
NM_001292063.2:c.7682C= MANE Select	NP_001278992.1:p.Ser2561=