Canonical Allele Identifier: CA1239824205

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460233_26460234delinsAG , CM000664.2:g.26460233_26460234delinsAG	GRCh38
NC_000002.11:g.26683101_26683102delinsAG , CM000664.1:g.26683101_26683102delinsAG	GRCh37
NC_000002.10:g.26536605_26536606delinsAG	NCBI36
NG_009937.1:g.103465_103466delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5814-29_5814-28delinsCT MANE Select	ENSP00000272371.2:n.5814-29_5814-28delinsCT
ENST00000339598.8:c.3512+413_3512+414delinsCT MANE Plus Clinical	ENSP00000344521.3:n.3512+413_3512+414delinsCT
ENST00000402415.8:c.3573-29_3573-28delinsCT	ENSP00000383906.4:n.3573-29_3573-28delinsCT
ENST00000272371.6:c.5814-29_5814-28delinsCT	ENSP00000272371.2:n.5814-29_5814-28delinsCT
ENST00000338581.10:c.3513-29_3513-28delinsCT	ENSP00000345137.6:n.3513-29_3513-28delinsCT
ENST00000339598.7:c.3512+413_3512+414delinsCT	ENSP00000344521.3:n.3512+413_3512+414delinsCT
ENST00000402415.7:c.3744-29_3744-28delinsCT	ENSP00000383906.3:n.3744-29_3744-28delinsCT
ENST00000403946.7:c.5813+413_5813+414delinsCT	ENSP00000385255.3:n.5813+413_5813+414delinsCT
NM_001287489.1:c.5813+413_5813+414delinsCT	NP_001274418.1:n.5813+413_5813+414delinsCT
NM_004802.3:c.3513-29_3513-28delinsCT	NP_004793.2:n.3513-29_3513-28delinsCT
NM_194248.2:c.5814-29_5814-28delinsCT	NP_919224.1:n.5814-29_5814-28delinsCT
NM_194322.2:c.3744-29_3744-28delinsCT	NP_919303.1:n.3744-29_3744-28delinsCT
NM_194323.2:c.3512+413_3512+414delinsCT	NP_919304.1:n.3512+413_3512+414delinsCT
XM_005264644.2:c.5798+413_5798+414delinsCT	XP_005264701.1:n.5798+413_5798+414delinsCT
XM_011533185.1:c.5858+413_5858+414delinsCT	XP_011531487.1:n.5858+413_5858+414delinsCT
XM_017005338.1:c.5754-29_5754-28delinsCT	XP_016860827.1:n.5754-29_5754-28delinsCT
NM_001287489.2:c.5813+413_5813+414delinsCT	NP_001274418.1:n.5813+413_5813+414delinsCT
NM_004802.4:c.3513-29_3513-28delinsCT	NP_004793.2:n.3513-29_3513-28delinsCT
NM_194248.3:c.5814-29_5814-28delinsCT MANE Select	NP_919224.1:n.5814-29_5814-28delinsCT
NM_194322.3:c.3744-29_3744-28delinsCT	NP_919303.1:n.3744-29_3744-28delinsCT
NM_194323.3:c.3512+413_3512+414delinsCT MANE Plus Clinical	NP_919304.1:n.3512+413_3512+414delinsCT