Canonical Allele Identifier: CA379783525

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17615598A>C (hg19) ; chr11:g.17594051A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17594051A>C , CM000673.2:g.17594051A>C	GRCh38
NC_000011.9:g.17615598A>C , CM000673.1:g.17615598A>C	GRCh37
NC_000011.8:g.17572174A>C	NCBI36
NG_033191.1:g.51679A>C
NG_033191.2:g.51679A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.3329A>C	ENSP00000382323.2:p.Gln1110Pro
ENST00000399397.6:c.3293A>C MANE Select	ENSP00000382329.2:p.Gln1098Pro
ENST00000342528.2:c.374A>C	ENSP00000341666.2:p.Gln125Pro
ENST00000399391.6:c.3329A>C	ENSP00000382323.2:p.Gln1110Pro
ENST00000399397.5:c.3293A>C	ENSP00000382329.2:p.Gln1098Pro
NM_001277269.1:c.3329A>C	NP_001264198.1:p.Gln1110Pro
NM_001292063.1:c.3293A>C	NP_001278992.1:p.Gln1098Pro
NM_001277269.2:c.3329A>C	NP_001264198.1:p.Gln1110Pro
NM_001292063.2:c.3293A>C MANE Select	NP_001278992.1:p.Gln1098Pro