Canonical Allele Identifier: CA379781077

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17660061G>C (hg19) ; chr11:g.17638514G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17638514G>C , CM000673.2:g.17638514G>C	GRCh38
NC_000011.9:g.17660061G>C , CM000673.1:g.17660061G>C	GRCh37
NC_000011.8:g.17616637G>C	NCBI36
NG_033191.1:g.96142G>C
NG_033191.2:g.96142G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7895G>C	ENSP00000382323.2:p.Trp2632Ser
ENST00000399397.6:c.7859G>C MANE Select	ENSP00000382329.2:p.Trp2620Ser
ENST00000342528.2:c.4487G>C	ENSP00000341666.2:p.Trp1496Ser
ENST00000399391.6:c.7895G>C	ENSP00000382323.2:p.Trp2632Ser
ENST00000399397.5:c.7859G>C	ENSP00000382329.2:p.Trp2620Ser
NM_001277269.1:c.7895G>C	NP_001264198.1:p.Trp2632Ser
NM_001292063.1:c.7859G>C	NP_001278992.1:p.Trp2620Ser
NM_001277269.2:c.7895G>C	NP_001264198.1:p.Trp2632Ser
NM_001292063.2:c.7859G>C MANE Select	NP_001278992.1:p.Trp2620Ser