Canonical Allele Identifier: CA2658238908

Gene: OTOF

Linked Data

• gnomAD v4: 2-26482659-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482660_26482661insTT , CM000664.2:g.26482660_26482661insTT	GRCh38
NC_000002.11:g.26705528_26705529insTT , CM000664.1:g.26705528_26705529insTT	GRCh37
NC_000002.10:g.26559032_26559033insTT	NCBI36
NG_009937.1:g.81039_81040insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-68_1393-67insAA MANE Select	ENSP00000272371.2:n.1393-68_1393-67insAA
ENST00000272371.6:c.1393-68_1393-67insAA	ENSP00000272371.2:n.1393-68_1393-67insAA
ENST00000403946.7:c.1393-68_1393-67insAA	ENSP00000385255.3:n.1393-68_1393-67insAA
NM_001287489.1:c.1393-68_1393-67insAA	NP_001274418.1:n.1393-68_1393-67insAA
NM_194248.2:c.1393-68_1393-67insAA	NP_919224.1:n.1393-68_1393-67insAA
XM_005264644.2:c.1438-68_1438-67insAA	XP_005264701.1:n.1438-68_1438-67insAA
XM_011533185.1:c.1438-68_1438-67insAA	XP_011531487.1:n.1438-68_1438-67insAA
XM_017005338.1:c.1393-68_1393-67insAA	XP_016860827.1:n.1393-68_1393-67insAA
NM_001287489.2:c.1393-68_1393-67insAA	NP_001274418.1:n.1393-68_1393-67insAA
NM_194248.3:c.1393-68_1393-67insAA MANE Select	NP_919224.1:n.1393-68_1393-67insAA