Canonical Allele Identifier: CA2658234782

Gene: OTOF

Linked Data

• gnomAD v4: 2-26467043-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467043_26467044insC , CM000664.2:g.26467043_26467044insC	GRCh38
NC_000002.11:g.26689911_26689912insC , CM000664.1:g.26689911_26689912insC	GRCh37
NC_000002.10:g.26543415_26543416insC	NCBI36
NG_009937.1:g.96655_96656insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4362+55_4362+56insG MANE Select	ENSP00000272371.2:n.4362+55_4362+56insG
ENST00000339598.8:c.2061+55_2061+56insG MANE Plus Clinical	ENSP00000344521.3:n.2061+55_2061+56insG
ENST00000402415.8:c.2121+55_2121+56insG	ENSP00000383906.4:n.2121+55_2121+56insG
ENST00000272371.6:c.4362+55_4362+56insG	ENSP00000272371.2:n.4362+55_4362+56insG
ENST00000338581.10:c.2061+55_2061+56insG	ENSP00000345137.6:n.2061+55_2061+56insG
ENST00000339598.7:c.2061+55_2061+56insG	ENSP00000344521.3:n.2061+55_2061+56insG
ENST00000402415.7:c.2292+55_2292+56insG	ENSP00000383906.3:n.2292+55_2292+56insG
ENST00000403946.7:c.4362+55_4362+56insG	ENSP00000385255.3:n.4362+55_4362+56insG
NM_001287489.1:c.4362+55_4362+56insG	NP_001274418.1:n.4362+55_4362+56insG
NM_004802.3:c.2061+55_2061+56insG	NP_004793.2:n.2061+55_2061+56insG
NM_194248.2:c.4362+55_4362+56insG	NP_919224.1:n.4362+55_4362+56insG
NM_194322.2:c.2292+55_2292+56insG	NP_919303.1:n.2292+55_2292+56insG
NM_194323.2:c.2061+55_2061+56insG	NP_919304.1:n.2061+55_2061+56insG
XM_005264644.2:c.4347+55_4347+56insG	XP_005264701.1:n.4347+55_4347+56insG
XM_011533185.1:c.4407+55_4407+56insG	XP_011531487.1:n.4407+55_4407+56insG
XM_017005338.1:c.4302+55_4302+56insG	XP_016860827.1:n.4302+55_4302+56insG
NM_001287489.2:c.4362+55_4362+56insG	NP_001274418.1:n.4362+55_4362+56insG
NM_004802.4:c.2061+55_2061+56insG	NP_004793.2:n.2061+55_2061+56insG
NM_194248.3:c.4362+55_4362+56insG MANE Select	NP_919224.1:n.4362+55_4362+56insG
NM_194322.3:c.2292+55_2292+56insG	NP_919303.1:n.2292+55_2292+56insG
NM_194323.3:c.2061+55_2061+56insG MANE Plus Clinical	NP_919304.1:n.2061+55_2061+56insG