Canonical Allele Identifier: CA1955242292

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17645758C= , CM000673.2:g.17645758C=	GRCh38
NC_000011.9:g.17667305C= , CM000673.1:g.17667305C=	GRCh37
NC_000011.8:g.17623881C=	NCBI36
NG_033191.1:g.103386C=
NG_033191.2:g.103386C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.8592C=	ENSP00000382323.2:p.Ser2864=
ENST00000399397.6:c.8556C= MANE Select	ENSP00000382329.2:p.Ser2852=
ENST00000399391.6:c.8592C=	ENSP00000382323.2:p.Ser2864=
ENST00000399397.5:c.8556C=	ENSP00000382329.2:p.Ser2852=
NM_001277269.1:c.8592C=	NP_001264198.1:p.Ser2864=
NM_001292063.1:c.8556C=	NP_001278992.1:p.Ser2852=
NM_001277269.2:c.8592C=	NP_001264198.1:p.Ser2864=
NM_001292063.2:c.8556C= MANE Select	NP_001278992.1:p.Ser2852=