Canonical Allele Identifier: CA1239825312

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26461566_26461567delinsCT , CM000664.2:g.26461566_26461567delinsCT	GRCh38
NC_000002.11:g.26684434_26684435delinsCT , CM000664.1:g.26684434_26684435delinsCT	GRCh37
NC_000002.10:g.26537938_26537939delinsCT	NCBI36
NG_009937.1:g.102132_102133delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5533+129_5533+130delinsAG MANE Select	ENSP00000272371.2:n.5533+129_5533+130delinsAG
ENST00000339598.8:c.3232+129_3232+130delinsAG MANE Plus Clinical	ENSP00000344521.3:n.3232+129_3232+130delinsAG
ENST00000402415.8:c.3292+129_3292+130delinsAG	ENSP00000383906.4:n.3292+129_3292+130delinsAG
ENST00000272371.6:c.5533+129_5533+130delinsAG	ENSP00000272371.2:n.5533+129_5533+130delinsAG
ENST00000338581.10:c.3232+129_3232+130delinsAG	ENSP00000345137.6:n.3232+129_3232+130delinsAG
ENST00000339598.7:c.3232+129_3232+130delinsAG	ENSP00000344521.3:n.3232+129_3232+130delinsAG
ENST00000402415.7:c.3463+129_3463+130delinsAG	ENSP00000383906.3:n.3463+129_3463+130delinsAG
ENST00000403946.7:c.5533+129_5533+130delinsAG	ENSP00000385255.3:n.5533+129_5533+130delinsAG
NM_001287489.1:c.5533+129_5533+130delinsAG	NP_001274418.1:n.5533+129_5533+130delinsAG
NM_004802.3:c.3232+129_3232+130delinsAG	NP_004793.2:n.3232+129_3232+130delinsAG
NM_194248.2:c.5533+129_5533+130delinsAG	NP_919224.1:n.5533+129_5533+130delinsAG
NM_194322.2:c.3463+129_3463+130delinsAG	NP_919303.1:n.3463+129_3463+130delinsAG
NM_194323.2:c.3232+129_3232+130delinsAG	NP_919304.1:n.3232+129_3232+130delinsAG
XM_005264644.2:c.5518+129_5518+130delinsAG	XP_005264701.1:n.5518+129_5518+130delinsAG
XM_011533185.1:c.5578+129_5578+130delinsAG	XP_011531487.1:n.5578+129_5578+130delinsAG
XM_017005338.1:c.5473+129_5473+130delinsAG	XP_016860827.1:n.5473+129_5473+130delinsAG
NM_001287489.2:c.5533+129_5533+130delinsAG	NP_001274418.1:n.5533+129_5533+130delinsAG
NM_004802.4:c.3232+129_3232+130delinsAG	NP_004793.2:n.3232+129_3232+130delinsAG
NM_194248.3:c.5533+129_5533+130delinsAG MANE Select	NP_919224.1:n.5533+129_5533+130delinsAG
NM_194322.3:c.3463+129_3463+130delinsAG	NP_919303.1:n.3463+129_3463+130delinsAG
NM_194323.3:c.3232+129_3232+130delinsAG MANE Plus Clinical	NP_919304.1:n.3232+129_3232+130delinsAG