Canonical Allele Identifier: CA2567515070

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26480636_26480637insTCGCACAGCACGTCGTAACG , CM000664.2:g.26480636_26480637insTCGCACAGCACGTCGTAACG	GRCh38
NC_000002.11:g.26703504_26703505insTCGCACAGCACGTCGTAACG , CM000664.1:g.26703504_26703505insTCGCACAGCACGTCGTAACG	GRCh37
NC_000002.10:g.26557008_26557009insTCGCACAGCACGTCGTAACG	NCBI36
NG_009937.1:g.83063_83064insGTTACGACGTGCTGTGCGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.1803+150_1803+151insGTTACGACGTGCTGTGCGAC MANE Select	ENSP00000272371.2:n.1803+150_1803+151insGTTACGACGTGCTGTGCGAC
ENST00000272371.6:c.1803+150_1803+151insGTTACGACGTGCTGTGCGAC	ENSP00000272371.2:n.1803+150_1803+151insGTTACGACGTGCTGTGCGAC
ENST00000403946.7:c.1803+150_1803+151insGTTACGACGTGCTGTGCGAC	ENSP00000385255.3:n.1803+150_1803+151insGTTACGACGTGCTGTGCGAC
NM_001287489.1:c.1803+150_1803+151insGTTACGACGTGCTGTGCGAC	NP_001274418.1:n.1803+150_1803+151insGTTACGACGTGCTGTGCGAC
NM_194248.2:c.1803+150_1803+151insGTTACGACGTGCTGTGCGAC	NP_919224.1:n.1803+150_1803+151insGTTACGACGTGCTGTGCGAC
XM_005264644.2:c.1848+150_1848+151insGTTACGACGTGCTGTGCGAC	XP_005264701.1:n.1848+150_1848+151insGTTACGACGTGCTGTGCGAC
XM_011533185.1:c.1848+150_1848+151insGTTACGACGTGCTGTGCGAC	XP_011531487.1:n.1848+150_1848+151insGTTACGACGTGCTGTGCGAC
XM_017005338.1:c.1803+150_1803+151insGTTACGACGTGCTGTGCGAC	XP_016860827.1:n.1803+150_1803+151insGTTACGACGTGCTGTGCGAC
NM_001287489.2:c.1803+150_1803+151insGTTACGACGTGCTGTGCGAC	NP_001274418.1:n.1803+150_1803+151insGTTACGACGTGCTGTGCGAC
NM_194248.3:c.1803+150_1803+151insGTTACGACGTGCTGTGCGAC MANE Select	NP_919224.1:n.1803+150_1803+151insGTTACGACGTGCTGTGCGAC