Canonical Allele Identifier: CA2658234785

Gene: OTOF

Linked Data

• gnomAD v4: 2-26467044-T-TGGGGGGGACCCTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467051_26467052insACCCTGGGGGGGGG , CM000664.2:g.26467051_26467052insACCCTGGGGGGGGG	GRCh38
NC_000002.11:g.26689919_26689920insACCCTGGGGGGGGG , CM000664.1:g.26689919_26689920insACCCTGGGGGGGGG	GRCh37
NC_000002.10:g.26543423_26543424insACCCTGGGGGGGGG	NCBI36
NG_009937.1:g.96654_96655insCCAGGGTCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4362+54_4362+55insCCAGGGTCCCCCCC MANE Select	ENSP00000272371.2:n.4362+54_4362+55insCCAGGGTCCCCCCC
ENST00000339598.8:c.2061+54_2061+55insCCAGGGTCCCCCCC MANE Plus Clinical	ENSP00000344521.3:n.2061+54_2061+55insCCAGGGTCCCCCCC
ENST00000402415.8:c.2121+54_2121+55insCCAGGGTCCCCCCC	ENSP00000383906.4:n.2121+54_2121+55insCCAGGGTCCCCCCC
ENST00000272371.6:c.4362+54_4362+55insCCAGGGTCCCCCCC	ENSP00000272371.2:n.4362+54_4362+55insCCAGGGTCCCCCCC
ENST00000338581.10:c.2061+54_2061+55insCCAGGGTCCCCCCC	ENSP00000345137.6:n.2061+54_2061+55insCCAGGGTCCCCCCC
ENST00000339598.7:c.2061+54_2061+55insCCAGGGTCCCCCCC	ENSP00000344521.3:n.2061+54_2061+55insCCAGGGTCCCCCCC
ENST00000402415.7:c.2292+54_2292+55insCCAGGGTCCCCCCC	ENSP00000383906.3:n.2292+54_2292+55insCCAGGGTCCCCCCC
ENST00000403946.7:c.4362+54_4362+55insCCAGGGTCCCCCCC	ENSP00000385255.3:n.4362+54_4362+55insCCAGGGTCCCCCCC
NM_001287489.1:c.4362+54_4362+55insCCAGGGTCCCCCCC	NP_001274418.1:n.4362+54_4362+55insCCAGGGTCCCCCCC
NM_004802.3:c.2061+54_2061+55insCCAGGGTCCCCCCC	NP_004793.2:n.2061+54_2061+55insCCAGGGTCCCCCCC
NM_194248.2:c.4362+54_4362+55insCCAGGGTCCCCCCC	NP_919224.1:n.4362+54_4362+55insCCAGGGTCCCCCCC
NM_194322.2:c.2292+54_2292+55insCCAGGGTCCCCCCC	NP_919303.1:n.2292+54_2292+55insCCAGGGTCCCCCCC
NM_194323.2:c.2061+54_2061+55insCCAGGGTCCCCCCC	NP_919304.1:n.2061+54_2061+55insCCAGGGTCCCCCCC
XM_005264644.2:c.4347+54_4347+55insCCAGGGTCCCCCCC	XP_005264701.1:n.4347+54_4347+55insCCAGGGTCCCCCCC
XM_011533185.1:c.4407+54_4407+55insCCAGGGTCCCCCCC	XP_011531487.1:n.4407+54_4407+55insCCAGGGTCCCCCCC
XM_017005338.1:c.4302+54_4302+55insCCAGGGTCCCCCCC	XP_016860827.1:n.4302+54_4302+55insCCAGGGTCCCCCCC
NM_001287489.2:c.4362+54_4362+55insCCAGGGTCCCCCCC	NP_001274418.1:n.4362+54_4362+55insCCAGGGTCCCCCCC
NM_004802.4:c.2061+54_2061+55insCCAGGGTCCCCCCC	NP_004793.2:n.2061+54_2061+55insCCAGGGTCCCCCCC
NM_194248.3:c.4362+54_4362+55insCCAGGGTCCCCCCC MANE Select	NP_919224.1:n.4362+54_4362+55insCCAGGGTCCCCCCC
NM_194322.3:c.2292+54_2292+55insCCAGGGTCCCCCCC	NP_919303.1:n.2292+54_2292+55insCCAGGGTCCCCCCC
NM_194323.3:c.2061+54_2061+55insCCAGGGTCCCCCCC MANE Plus Clinical	NP_919304.1:n.2061+54_2061+55insCCAGGGTCCCCCCC