Canonical Allele Identifier: CA2658238900

Gene: OTOF

Linked Data

• gnomAD v4: 2-26482652-T-TGTGTGTGTGAGTGGGCGC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482653_26482670dup , CM000664.2:g.26482653_26482670dup	GRCh38
NC_000002.11:g.26705521_26705538dup , CM000664.1:g.26705521_26705538dup	GRCh37
NC_000002.10:g.26559025_26559042dup	NCBI36
NG_009937.1:g.81029_81046dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-78_1393-61dup MANE Select	ENSP00000272371.2:n.1393-78_1393-61dup
ENST00000272371.6:c.1393-78_1393-61dup	ENSP00000272371.2:n.1393-78_1393-61dup
ENST00000403946.7:c.1393-78_1393-61dup	ENSP00000385255.3:n.1393-78_1393-61dup
NM_001287489.1:c.1393-78_1393-61dup	NP_001274418.1:n.1393-78_1393-61dup
NM_194248.2:c.1393-78_1393-61dup	NP_919224.1:n.1393-78_1393-61dup
XM_005264644.2:c.1438-78_1438-61dup	XP_005264701.1:n.1438-78_1438-61dup
XM_011533185.1:c.1438-78_1438-61dup	XP_011531487.1:n.1438-78_1438-61dup
XM_017005338.1:c.1393-78_1393-61dup	XP_016860827.1:n.1393-78_1393-61dup
NM_001287489.2:c.1393-78_1393-61dup	NP_001274418.1:n.1393-78_1393-61dup
NM_194248.3:c.1393-78_1393-61dup MANE Select	NP_919224.1:n.1393-78_1393-61dup