Canonical Allele Identifier: CA2556433613

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467074_26467075insAGAT , CM000664.2:g.26467074_26467075insAGAT	GRCh38
NC_000002.11:g.26689942_26689943insAGAT , CM000664.1:g.26689942_26689943insAGAT	GRCh37
NC_000002.10:g.26543446_26543447insAGAT	NCBI36
NG_009937.1:g.96624_96625insATCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4362+24_4362+25insATCT MANE Select	ENSP00000272371.2:n.4362+24_4362+25insATCT
ENST00000339598.8:c.2061+24_2061+25insATCT MANE Plus Clinical	ENSP00000344521.3:n.2061+24_2061+25insATCT
ENST00000402415.8:c.2121+24_2121+25insATCT	ENSP00000383906.4:n.2121+24_2121+25insATCT
ENST00000272371.6:c.4362+24_4362+25insATCT	ENSP00000272371.2:n.4362+24_4362+25insATCT
ENST00000338581.10:c.2061+24_2061+25insATCT	ENSP00000345137.6:n.2061+24_2061+25insATCT
ENST00000339598.7:c.2061+24_2061+25insATCT	ENSP00000344521.3:n.2061+24_2061+25insATCT
ENST00000402415.7:c.2292+24_2292+25insATCT	ENSP00000383906.3:n.2292+24_2292+25insATCT
ENST00000403946.7:c.4362+24_4362+25insATCT	ENSP00000385255.3:n.4362+24_4362+25insATCT
NM_001287489.1:c.4362+24_4362+25insATCT	NP_001274418.1:n.4362+24_4362+25insATCT
NM_004802.3:c.2061+24_2061+25insATCT	NP_004793.2:n.2061+24_2061+25insATCT
NM_194248.2:c.4362+24_4362+25insATCT	NP_919224.1:n.4362+24_4362+25insATCT
NM_194322.2:c.2292+24_2292+25insATCT	NP_919303.1:n.2292+24_2292+25insATCT
NM_194323.2:c.2061+24_2061+25insATCT	NP_919304.1:n.2061+24_2061+25insATCT
XM_005264644.2:c.4347+24_4347+25insATCT	XP_005264701.1:n.4347+24_4347+25insATCT
XM_011533185.1:c.4407+24_4407+25insATCT	XP_011531487.1:n.4407+24_4407+25insATCT
XM_017005338.1:c.4302+24_4302+25insATCT	XP_016860827.1:n.4302+24_4302+25insATCT
NM_001287489.2:c.4362+24_4362+25insATCT	NP_001274418.1:n.4362+24_4362+25insATCT
NM_004802.4:c.2061+24_2061+25insATCT	NP_004793.2:n.2061+24_2061+25insATCT
NM_194248.3:c.4362+24_4362+25insATCT MANE Select	NP_919224.1:n.4362+24_4362+25insATCT
NM_194322.3:c.2292+24_2292+25insATCT	NP_919303.1:n.2292+24_2292+25insATCT
NM_194323.3:c.2061+24_2061+25insATCT MANE Plus Clinical	NP_919304.1:n.2061+24_2061+25insATCT