Canonical Allele Identifier: CA1955197638

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553208A= , CM000673.2:g.17553208A=	GRCh38
NC_000011.9:g.17574755A= , CM000673.1:g.17574755A=	GRCh37
NC_000011.8:g.17531331A=	NCBI36
NG_033191.1:g.10836A=
NG_033191.2:g.10836A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.418A=	ENSP00000382323.2:p.Met140=
ENST00000399397.6:c.382A= MANE Select	ENSP00000382329.2:p.Met128=
ENST00000399391.6:c.418A=	ENSP00000382323.2:p.Met140=
ENST00000399397.5:c.382A=	ENSP00000382329.2:p.Met128=
ENST00000428619.1:c.199A=	ENSP00000399057.2:p.Met67=
ENST00000498332.5:n.288A=
NM_001277269.1:c.418A=	NP_001264198.1:p.Met140=
NM_001292063.1:c.382A=	NP_001278992.1:p.Met128=
NM_001277269.2:c.418A=	NP_001264198.1:p.Met140=
NM_001292063.2:c.382A= MANE Select	NP_001278992.1:p.Met128=