Canonical Allele Identifier: CA1955197738

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553373G= , CM000673.2:g.17553373G=	GRCh38
NC_000011.9:g.17574920G= , CM000673.1:g.17574920G=	GRCh37
NC_000011.8:g.17531496G=	NCBI36
NG_033191.1:g.11001G=
NG_033191.2:g.11001G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.430G=	ENSP00000382323.2:p.Ala144=
ENST00000399397.6:c.394G= MANE Select	ENSP00000382329.2:p.Ala132=
ENST00000399391.6:c.430G=	ENSP00000382323.2:p.Ala144=
ENST00000399397.5:c.394G=	ENSP00000382329.2:p.Ala132=
ENST00000428619.1:c.211G=	ENSP00000399057.2:p.Ala71=
ENST00000498332.5:n.300G=
NM_001277269.1:c.430G=	NP_001264198.1:p.Ala144=
NM_001292063.1:c.394G=	NP_001278992.1:p.Ala132=
NM_001277269.2:c.430G=	NP_001264198.1:p.Ala144=
NM_001292063.2:c.394G= MANE Select	NP_001278992.1:p.Ala132=