Canonical Allele Identifier: CA2658234791

Gene: OTOF

Linked Data

• gnomAD v4: 2-26467052-G-GCGGGGGGGACCCGGGGGGGGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467053_26467054insGGGGGGGACCCGGGGGGGGGGCC , CM000664.2:g.26467053_26467054insGGGGGGGACCCGGGGGGGGGGCC	GRCh38
NC_000002.11:g.26689921_26689922insGGGGGGGACCCGGGGGGGGGGCC , CM000664.1:g.26689921_26689922insGGGGGGGACCCGGGGGGGGGGCC	GRCh37
NC_000002.10:g.26543425_26543426insGGGGGGGACCCGGGGGGGGGGCC	NCBI36
NG_009937.1:g.96646_96647insGCCCCCCCCCCGGGTCCCCCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG MANE Select	ENSP00000272371.2:n.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG...
ENST00000339598.8:c.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG MANE Plus Clinical	ENSP00000344521.3:n.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG...
ENST00000402415.8:c.2121+46_2121+47insGCCCCCCCCCCGGGTCCCCCCCG	ENSP00000383906.4:n.2121+46_2121+47insGCCCCCCCCCCGGGTCCCCCCCG...
ENST00000272371.6:c.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG	ENSP00000272371.2:n.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG...
ENST00000338581.10:c.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG	ENSP00000345137.6:n.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG...
ENST00000339598.7:c.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG	ENSP00000344521.3:n.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG...
ENST00000402415.7:c.2292+46_2292+47insGCCCCCCCCCCGGGTCCCCCCCG	ENSP00000383906.3:n.2292+46_2292+47insGCCCCCCCCCCGGGTCCCCCCCG...
ENST00000403946.7:c.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG	ENSP00000385255.3:n.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG...
NM_001287489.1:c.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG	NP_001274418.1:n.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_004802.3:c.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG	NP_004793.2:n.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_194248.2:c.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG	NP_919224.1:n.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_194322.2:c.2292+46_2292+47insGCCCCCCCCCCGGGTCCCCCCCG	NP_919303.1:n.2292+46_2292+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_194323.2:c.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG	NP_919304.1:n.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG
XM_005264644.2:c.4347+46_4347+47insGCCCCCCCCCCGGGTCCCCCCCG	XP_005264701.1:n.4347+46_4347+47insGCCCCCCCCCCGGGTCCCCCCCG
XM_011533185.1:c.4407+46_4407+47insGCCCCCCCCCCGGGTCCCCCCCG	XP_011531487.1:n.4407+46_4407+47insGCCCCCCCCCCGGGTCCCCCCCG
XM_017005338.1:c.4302+46_4302+47insGCCCCCCCCCCGGGTCCCCCCCG	XP_016860827.1:n.4302+46_4302+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_001287489.2:c.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG	NP_001274418.1:n.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_004802.4:c.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG	NP_004793.2:n.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_194248.3:c.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG MANE Select	NP_919224.1:n.4362+46_4362+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_194322.3:c.2292+46_2292+47insGCCCCCCCCCCGGGTCCCCCCCG	NP_919303.1:n.2292+46_2292+47insGCCCCCCCCCCGGGTCCCCCCCG
NM_194323.3:c.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG MANE Plus Clinical	NP_919304.1:n.2061+46_2061+47insGCCCCCCCCCCGGGTCCCCCCCG