Canonical Allele Identifier: CA2571293499

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26480640_26480641insGCGGCGACCGCCCTGCATGGCGTAGGAAACGCTGGCGGTGACGACGGAAAACACTATGCCCATGCCCACGCCAAGAA , CM000664.2:g.26480640_26480641insGCGGCGACCGCCCTGCATGGCGTAGGAAACGCTGGCGGTGACGACGGAAAACACTATGCCCATGCCCACGCCAAGAA	GRCh38
NC_000002.11:g.26703508_26703509insGCGGCGACCGCCCTGCATGGCGTAGGAAACGCTGGCGGTGACGACGGAAAACACTATGCCCATGCCCACGCCAAGAA , CM000664.1:g.26703508_26703509insGCGGCGACCGCCCTGCATGGCGTAGGAAACGCTGGCGGTGACGACGGAAAACACTATGCCCATGCCCACGCCAAGAA	GRCh37
NC_000002.10:g.26557012_26557013insGCGGCGACCGCCCTGCATGGCGTAGGAAACGCTGGCGGTGACGACGGAAAACACTATGCCCATGCCCACGCCAAGAA	NCBI36
NG_009937.1:g.83058_83059insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC MANE Select	ENSP00000272371.2:n.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCA...
ENST00000272371.6:c.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC	ENSP00000272371.2:n.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCA...
ENST00000403946.7:c.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC	ENSP00000385255.3:n.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCA...
NM_001287489.1:c.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC	NP_001274418.1:n.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAG...
NM_194248.2:c.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC	NP_919224.1:n.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGT...
XM_005264644.2:c.1848+145_1848+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC	XP_005264701.1:n.1848+145_1848+146insTTCTTGGCGTGGGCATGGGCATAG...
XM_011533185.1:c.1848+145_1848+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC	XP_011531487.1:n.1848+145_1848+146insTTCTTGGCGTGGGCATGGGCATAG...
XM_017005338.1:c.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC	XP_016860827.1:n.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAG...
NM_001287489.2:c.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC	NP_001274418.1:n.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAG...
NM_194248.3:c.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGTTTTCCGTCGTCACCGCCAGCGTTTCCTACGCCATGCAGGGCGGTCGCCGC MANE Select	NP_919224.1:n.1803+145_1803+146insTTCTTGGCGTGGGCATGGGCATAGTGT...