Canonical Allele Identifier: CA2573051914

Gene: OTOF

Linked Data

• ClinVar Variation Id: 1185100
• ClinVar RCV Id: RCV001822922 ; RCV003483833
• dbSNP Id: rs2148051770

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26477414dup , CM000664.2:g.26477414dup	GRCh38
NC_000002.11:g.26700282dup , CM000664.1:g.26700282dup	GRCh37
NC_000002.10:g.26553786dup	NCBI36
NG_009937.1:g.86285dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.2406+2dup MANE Select	ENSP00000272371.2:n.2406+2dup
ENST00000339598.8:c.165+2dup MANE Plus Clinical	ENSP00000344521.3:n.165+2dup
ENST00000402415.8:c.165+2dup	ENSP00000383906.4:n.165+2dup
ENST00000272371.6:c.2406+2dup	ENSP00000272371.2:n.2406+2dup
ENST00000338581.10:c.165+2dup	ENSP00000345137.6:n.165+2dup
ENST00000339598.7:c.165+2dup	ENSP00000344521.3:n.165+2dup
ENST00000402415.7:c.336+2dup	ENSP00000383906.3:n.336+2dup
ENST00000403946.7:c.2406+2dup	ENSP00000385255.3:n.2406+2dup
NM_001287489.1:c.2406+2dup	NP_001274418.1:n.2406+2dup
NM_004802.3:c.165+2dup	NP_004793.2:n.165+2dup
NM_194248.2:c.2406+2dup	NP_919224.1:n.2406+2dup
NM_194322.2:c.336+2dup	NP_919303.1:n.336+2dup
NM_194323.2:c.165+2dup	NP_919304.1:n.165+2dup
XM_005264644.2:c.2451+2dup	XP_005264701.1:n.2451+2dup
XM_011533185.1:c.2451+2dup	XP_011531487.1:n.2451+2dup
XM_017005338.1:c.2406+2dup	XP_016860827.1:n.2406+2dup
NM_001287489.2:c.2406+2dup	NP_001274418.1:n.2406+2dup
NM_004802.4:c.165+2dup	NP_004793.2:n.165+2dup
NM_194248.3:c.2406+2dup MANE Select	NP_919224.1:n.2406+2dup
NM_194322.3:c.336+2dup	NP_919303.1:n.336+2dup
NM_194323.3:c.165+2dup MANE Plus Clinical	NP_919304.1:n.165+2dup