Canonical Allele Identifier: CA1955238529

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17638471C= , CM000673.2:g.17638471C=	GRCh38
NC_000011.9:g.17660018C= , CM000673.1:g.17660018C=	GRCh37
NC_000011.8:g.17616594C=	NCBI36
NG_033191.1:g.96099C=
NG_033191.2:g.96099C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7852C=	ENSP00000382323.2:p.Pro2618=
ENST00000399397.6:c.7816C= MANE Select	ENSP00000382329.2:p.Pro2606=
ENST00000342528.2:c.4444C=	ENSP00000341666.2:p.Pro1482=
ENST00000399391.6:c.7852C=	ENSP00000382323.2:p.Pro2618=
ENST00000399397.5:c.7816C=	ENSP00000382329.2:p.Pro2606=
NM_001277269.1:c.7852C=	NP_001264198.1:p.Pro2618=
NM_001292063.1:c.7816C=	NP_001278992.1:p.Pro2606=
NM_001277269.2:c.7852C=	NP_001264198.1:p.Pro2618=
NM_001292063.2:c.7816C= MANE Select	NP_001278992.1:p.Pro2606=