Canonical Allele Identifier: CA2658234772

Gene: OTOF

Linked Data

• gnomAD v4: 2-26467028-TGAGTGGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467031_26467038del , CM000664.2:g.26467031_26467038del	GRCh38
NC_000002.11:g.26689899_26689906del , CM000664.1:g.26689899_26689906del	GRCh37
NC_000002.10:g.26543403_26543410del	NCBI36
NG_009937.1:g.96663_96670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4362+63_4362+70del MANE Select	ENSP00000272371.2:n.4362+63_4362+70del
ENST00000339598.8:c.2061+63_2061+70del MANE Plus Clinical	ENSP00000344521.3:n.2061+63_2061+70del
ENST00000402415.8:c.2121+63_2121+70del	ENSP00000383906.4:n.2121+63_2121+70del
ENST00000272371.6:c.4362+63_4362+70del	ENSP00000272371.2:n.4362+63_4362+70del
ENST00000338581.10:c.2061+63_2061+70del	ENSP00000345137.6:n.2061+63_2061+70del
ENST00000339598.7:c.2061+63_2061+70del	ENSP00000344521.3:n.2061+63_2061+70del
ENST00000402415.7:c.2292+63_2292+70del	ENSP00000383906.3:n.2292+63_2292+70del
ENST00000403946.7:c.4362+63_4362+70del	ENSP00000385255.3:n.4362+63_4362+70del
NM_001287489.1:c.4362+63_4362+70del	NP_001274418.1:n.4362+63_4362+70del
NM_004802.3:c.2061+63_2061+70del	NP_004793.2:n.2061+63_2061+70del
NM_194248.2:c.4362+63_4362+70del	NP_919224.1:n.4362+63_4362+70del
NM_194322.2:c.2292+63_2292+70del	NP_919303.1:n.2292+63_2292+70del
NM_194323.2:c.2061+63_2061+70del	NP_919304.1:n.2061+63_2061+70del
XM_005264644.2:c.4347+63_4347+70del	XP_005264701.1:n.4347+63_4347+70del
XM_011533185.1:c.4407+63_4407+70del	XP_011531487.1:n.4407+63_4407+70del
XM_017005338.1:c.4302+63_4302+70del	XP_016860827.1:n.4302+63_4302+70del
NM_001287489.2:c.4362+63_4362+70del	NP_001274418.1:n.4362+63_4362+70del
NM_004802.4:c.2061+63_2061+70del	NP_004793.2:n.2061+63_2061+70del
NM_194248.3:c.4362+63_4362+70del MANE Select	NP_919224.1:n.4362+63_4362+70del
NM_194322.3:c.2292+63_2292+70del	NP_919303.1:n.2292+63_2292+70del
NM_194323.3:c.2061+63_2061+70del MANE Plus Clinical	NP_919304.1:n.2061+63_2061+70del