Canonical Allele Identifier: CA2658239947

Gene: OTOF

Linked Data

• gnomAD v4: 2-26484433-G-GGCTGGCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484434_26484441dup , CM000664.2:g.26484434_26484441dup	GRCh38
NC_000002.11:g.26707302_26707309dup , CM000664.1:g.26707302_26707309dup	GRCh37
NC_000002.10:g.26560806_26560813dup	NCBI36
NG_009937.1:g.79258_79265dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1205+33_1205+40dup MANE Select	ENSP00000272371.2:n.1205+33_1205+40dup
ENST00000272371.6:c.1205+33_1205+40dup	ENSP00000272371.2:n.1205+33_1205+40dup
ENST00000403946.7:c.1205+33_1205+40dup	ENSP00000385255.3:n.1205+33_1205+40dup
NM_001287489.1:c.1205+33_1205+40dup	NP_001274418.1:n.1205+33_1205+40dup
NM_194248.2:c.1205+33_1205+40dup	NP_919224.1:n.1205+33_1205+40dup
XM_005264644.2:c.1250+33_1250+40dup	XP_005264701.1:n.1250+33_1250+40dup
XM_011533185.1:c.1250+33_1250+40dup	XP_011531487.1:n.1250+33_1250+40dup
XM_017005338.1:c.1205+33_1205+40dup	XP_016860827.1:n.1205+33_1205+40dup
NM_001287489.2:c.1205+33_1205+40dup	NP_001274418.1:n.1205+33_1205+40dup
NM_194248.3:c.1205+33_1205+40dup MANE Select	NP_919224.1:n.1205+33_1205+40dup