Canonical Allele Identifier: CA379812987

Gene: OTOG

Linked Data

• dbSNP Id: rs2133709732
• MyVariant Identifiers: chr11:g.17656669G>T (hg19) ; chr11:g.17635122G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635122G>T , CM000673.2:g.17635122G>T	GRCh38
NC_000011.9:g.17656669G>T , CM000673.1:g.17656669G>T	GRCh37
NC_000011.8:g.17613245G>T	NCBI36
NG_033191.1:g.92750G>T
NG_033191.2:g.92750G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7664G>T	ENSP00000382323.2:p.Cys2555Phe
ENST00000399397.6:c.7628G>T MANE Select	ENSP00000382329.2:p.Cys2543Phe
ENST00000342528.2:c.4322-488G>T	ENSP00000341666.2:n.4322-488G>T
ENST00000399391.6:c.7664G>T	ENSP00000382323.2:p.Cys2555Phe
ENST00000399397.5:c.7628G>T	ENSP00000382329.2:p.Cys2543Phe
NM_001277269.1:c.7664G>T	NP_001264198.1:p.Cys2555Phe
NM_001292063.1:c.7628G>T	NP_001278992.1:p.Cys2543Phe
NM_001277269.2:c.7664G>T	NP_001264198.1:p.Cys2555Phe
NM_001292063.2:c.7628G>T MANE Select	NP_001278992.1:p.Cys2543Phe