Canonical Allele Identifier: CA2538749090

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467075_26467076insGGAAGAGCG , CM000664.2:g.26467075_26467076insGGAAGAGCG	GRCh38
NC_000002.11:g.26689943_26689944insGGAAGAGCG , CM000664.1:g.26689943_26689944insGGAAGAGCG	GRCh37
NC_000002.10:g.26543447_26543448insGGAAGAGCG	NCBI36
NG_009937.1:g.96623_96624insCGCTCTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4362+23_4362+24insCGCTCTTCC MANE Select	ENSP00000272371.2:n.4362+23_4362+24insCGCTCTTCC
ENST00000339598.8:c.2061+23_2061+24insCGCTCTTCC MANE Plus Clinical	ENSP00000344521.3:n.2061+23_2061+24insCGCTCTTCC
ENST00000402415.8:c.2121+23_2121+24insCGCTCTTCC	ENSP00000383906.4:n.2121+23_2121+24insCGCTCTTCC
ENST00000272371.6:c.4362+23_4362+24insCGCTCTTCC	ENSP00000272371.2:n.4362+23_4362+24insCGCTCTTCC
ENST00000338581.10:c.2061+23_2061+24insCGCTCTTCC	ENSP00000345137.6:n.2061+23_2061+24insCGCTCTTCC
ENST00000339598.7:c.2061+23_2061+24insCGCTCTTCC	ENSP00000344521.3:n.2061+23_2061+24insCGCTCTTCC
ENST00000402415.7:c.2292+23_2292+24insCGCTCTTCC	ENSP00000383906.3:n.2292+23_2292+24insCGCTCTTCC
ENST00000403946.7:c.4362+23_4362+24insCGCTCTTCC	ENSP00000385255.3:n.4362+23_4362+24insCGCTCTTCC
NM_001287489.1:c.4362+23_4362+24insCGCTCTTCC	NP_001274418.1:n.4362+23_4362+24insCGCTCTTCC
NM_004802.3:c.2061+23_2061+24insCGCTCTTCC	NP_004793.2:n.2061+23_2061+24insCGCTCTTCC
NM_194248.2:c.4362+23_4362+24insCGCTCTTCC	NP_919224.1:n.4362+23_4362+24insCGCTCTTCC
NM_194322.2:c.2292+23_2292+24insCGCTCTTCC	NP_919303.1:n.2292+23_2292+24insCGCTCTTCC
NM_194323.2:c.2061+23_2061+24insCGCTCTTCC	NP_919304.1:n.2061+23_2061+24insCGCTCTTCC
XM_005264644.2:c.4347+23_4347+24insCGCTCTTCC	XP_005264701.1:n.4347+23_4347+24insCGCTCTTCC
XM_011533185.1:c.4407+23_4407+24insCGCTCTTCC	XP_011531487.1:n.4407+23_4407+24insCGCTCTTCC
XM_017005338.1:c.4302+23_4302+24insCGCTCTTCC	XP_016860827.1:n.4302+23_4302+24insCGCTCTTCC
NM_001287489.2:c.4362+23_4362+24insCGCTCTTCC	NP_001274418.1:n.4362+23_4362+24insCGCTCTTCC
NM_004802.4:c.2061+23_2061+24insCGCTCTTCC	NP_004793.2:n.2061+23_2061+24insCGCTCTTCC
NM_194248.3:c.4362+23_4362+24insCGCTCTTCC MANE Select	NP_919224.1:n.4362+23_4362+24insCGCTCTTCC
NM_194322.3:c.2292+23_2292+24insCGCTCTTCC	NP_919303.1:n.2292+23_2292+24insCGCTCTTCC
NM_194323.3:c.2061+23_2061+24insCGCTCTTCC MANE Plus Clinical	NP_919304.1:n.2061+23_2061+24insCGCTCTTCC