Canonical Allele Identifier: CA1239828608

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482100_26482101delinsGC , CM000664.2:g.26482100_26482101delinsGC	GRCh38
NC_000002.11:g.26704968_26704969delinsGC , CM000664.1:g.26704968_26704969delinsGC	GRCh37
NC_000002.10:g.26558472_26558473delinsGC	NCBI36
NG_009937.1:g.81598_81599delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1579+305_1579+306delinsGC MANE Select	ENSP00000272371.2:n.1579+305_1579+306delinsGC
ENST00000272371.6:c.1579+305_1579+306delinsGC	ENSP00000272371.2:n.1579+305_1579+306delinsGC
ENST00000403946.7:c.1579+305_1579+306delinsGC	ENSP00000385255.3:n.1579+305_1579+306delinsGC
NM_001287489.1:c.1579+305_1579+306delinsGC	NP_001274418.1:n.1579+305_1579+306delinsGC
NM_194248.2:c.1579+305_1579+306delinsGC	NP_919224.1:n.1579+305_1579+306delinsGC
XM_005264644.2:c.1624+305_1624+306delinsGC	XP_005264701.1:n.1624+305_1624+306delinsGC
XM_011533185.1:c.1624+305_1624+306delinsGC	XP_011531487.1:n.1624+305_1624+306delinsGC
XM_017005338.1:c.1579+305_1579+306delinsGC	XP_016860827.1:n.1579+305_1579+306delinsGC
NM_001287489.2:c.1579+305_1579+306delinsGC	NP_001274418.1:n.1579+305_1579+306delinsGC
NM_194248.3:c.1579+305_1579+306delinsGC MANE Select	NP_919224.1:n.1579+305_1579+306delinsGC