Canonical Allele Identifier: CA1239818318

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467310_26467311delinsGC , CM000664.2:g.26467310_26467311delinsGC	GRCh38
NC_000002.11:g.26690178_26690179delinsGC , CM000664.1:g.26690178_26690179delinsGC	GRCh37
NC_000002.10:g.26543682_26543683delinsGC	NCBI36
NG_009937.1:g.96388_96389delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4227+54_4227+55delinsGC MANE Select	ENSP00000272371.2:n.4227+54_4227+55delinsGC
ENST00000339598.8:c.1926+54_1926+55delinsGC MANE Plus Clinical	ENSP00000344521.3:n.1926+54_1926+55delinsGC
ENST00000402415.8:c.1986+54_1986+55delinsGC	ENSP00000383906.4:n.1986+54_1986+55delinsGC
ENST00000272371.6:c.4227+54_4227+55delinsGC	ENSP00000272371.2:n.4227+54_4227+55delinsGC
ENST00000338581.10:c.1926+54_1926+55delinsGC	ENSP00000345137.6:n.1926+54_1926+55delinsGC
ENST00000339598.7:c.1926+54_1926+55delinsGC	ENSP00000344521.3:n.1926+54_1926+55delinsGC
ENST00000402415.7:c.2157+54_2157+55delinsGC	ENSP00000383906.3:n.2157+54_2157+55delinsGC
ENST00000403946.7:c.4227+54_4227+55delinsGC	ENSP00000385255.3:n.4227+54_4227+55delinsGC
NM_001287489.1:c.4227+54_4227+55delinsGC	NP_001274418.1:n.4227+54_4227+55delinsGC
NM_004802.3:c.1926+54_1926+55delinsGC	NP_004793.2:n.1926+54_1926+55delinsGC
NM_194248.2:c.4227+54_4227+55delinsGC	NP_919224.1:n.4227+54_4227+55delinsGC
NM_194322.2:c.2157+54_2157+55delinsGC	NP_919303.1:n.2157+54_2157+55delinsGC
NM_194323.2:c.1926+54_1926+55delinsGC	NP_919304.1:n.1926+54_1926+55delinsGC
XM_005264644.2:c.4212+54_4212+55delinsGC	XP_005264701.1:n.4212+54_4212+55delinsGC
XM_011533185.1:c.4272+54_4272+55delinsGC	XP_011531487.1:n.4272+54_4272+55delinsGC
XM_017005338.1:c.4167+54_4167+55delinsGC	XP_016860827.1:n.4167+54_4167+55delinsGC
NM_001287489.2:c.4227+54_4227+55delinsGC	NP_001274418.1:n.4227+54_4227+55delinsGC
NM_004802.4:c.1926+54_1926+55delinsGC	NP_004793.2:n.1926+54_1926+55delinsGC
NM_194248.3:c.4227+54_4227+55delinsGC MANE Select	NP_919224.1:n.4227+54_4227+55delinsGC
NM_194322.3:c.2157+54_2157+55delinsGC	NP_919303.1:n.2157+54_2157+55delinsGC
NM_194323.3:c.1926+54_1926+55delinsGC MANE Plus Clinical	NP_919304.1:n.1926+54_1926+55delinsGC