Canonical Allele Identifier: CA1239829282

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482672_26482673delinsTG , CM000664.2:g.26482672_26482673delinsTG	GRCh38
NC_000002.11:g.26705540_26705541delinsTG , CM000664.1:g.26705540_26705541delinsTG	GRCh37
NC_000002.10:g.26559044_26559045delinsTG	NCBI36
NG_009937.1:g.81026_81027delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-81_1393-80delinsCA MANE Select	ENSP00000272371.2:n.1393-81_1393-80delinsCA
ENST00000272371.6:c.1393-81_1393-80delinsCA	ENSP00000272371.2:n.1393-81_1393-80delinsCA
ENST00000403946.7:c.1393-81_1393-80delinsCA	ENSP00000385255.3:n.1393-81_1393-80delinsCA
NM_001287489.1:c.1393-81_1393-80delinsCA	NP_001274418.1:n.1393-81_1393-80delinsCA
NM_194248.2:c.1393-81_1393-80delinsCA	NP_919224.1:n.1393-81_1393-80delinsCA
XM_005264644.2:c.1438-81_1438-80delinsCA	XP_005264701.1:n.1438-81_1438-80delinsCA
XM_011533185.1:c.1438-81_1438-80delinsCA	XP_011531487.1:n.1438-81_1438-80delinsCA
XM_017005338.1:c.1393-81_1393-80delinsCA	XP_016860827.1:n.1393-81_1393-80delinsCA
NM_001287489.2:c.1393-81_1393-80delinsCA	NP_001274418.1:n.1393-81_1393-80delinsCA
NM_194248.3:c.1393-81_1393-80delinsCA MANE Select	NP_919224.1:n.1393-81_1393-80delinsCA