Canonical Allele Identifier: CA767290316

Gene: OTOF

Linked Data

• dbSNP Id: rs1553354298
• MyVariant Identifiers: chr2:g.26705673_26705674insTGTA (hg19) ; chr2:g.26482805_26482806insTGTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482808_26482811dup , CM000664.2:g.26482808_26482811dup	GRCh38
NC_000002.11:g.26705676_26705679dup , CM000664.1:g.26705676_26705679dup	GRCh37
NC_000002.10:g.26559180_26559183dup	NCBI36
NG_009937.1:g.80890_80893dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-217_1393-214dup MANE Select	ENSP00000272371.2:n.1393-217_1393-214dup
ENST00000272371.6:c.1393-217_1393-214dup	ENSP00000272371.2:n.1393-217_1393-214dup
ENST00000403946.7:c.1393-217_1393-214dup	ENSP00000385255.3:n.1393-217_1393-214dup
NM_001287489.1:c.1393-217_1393-214dup	NP_001274418.1:n.1393-217_1393-214dup
NM_194248.2:c.1393-217_1393-214dup	NP_919224.1:n.1393-217_1393-214dup
XM_005264644.2:c.1438-217_1438-214dup	XP_005264701.1:n.1438-217_1438-214dup
XM_011533185.1:c.1438-217_1438-214dup	XP_011531487.1:n.1438-217_1438-214dup
XM_017005338.1:c.1393-217_1393-214dup	XP_016860827.1:n.1393-217_1393-214dup
NM_001287489.2:c.1393-217_1393-214dup	NP_001274418.1:n.1393-217_1393-214dup
NM_194248.3:c.1393-217_1393-214dup MANE Select	NP_919224.1:n.1393-217_1393-214dup