Canonical Allele Identifier: CA379780852

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17660033G>C (hg19) ; chr11:g.17638486G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17638486G>C , CM000673.2:g.17638486G>C	GRCh38
NC_000011.9:g.17660033G>C , CM000673.1:g.17660033G>C	GRCh37
NC_000011.8:g.17616609G>C	NCBI36
NG_033191.1:g.96114G>C
NG_033191.2:g.96114G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7867G>C	ENSP00000382323.2:p.Gly2623Arg
ENST00000399397.6:c.7831G>C MANE Select	ENSP00000382329.2:p.Gly2611Arg
ENST00000342528.2:c.4459G>C	ENSP00000341666.2:p.Gly1487Arg
ENST00000399391.6:c.7867G>C	ENSP00000382323.2:p.Gly2623Arg
ENST00000399397.5:c.7831G>C	ENSP00000382329.2:p.Gly2611Arg
NM_001277269.1:c.7867G>C	NP_001264198.1:p.Gly2623Arg
NM_001292063.1:c.7831G>C	NP_001278992.1:p.Gly2611Arg
NM_001277269.2:c.7867G>C	NP_001264198.1:p.Gly2623Arg
NM_001292063.2:c.7831G>C MANE Select	NP_001278992.1:p.Gly2611Arg