Canonical Allele Identifier: CA1239828641

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482130_26482133delinsAATC , CM000664.2:g.26482130_26482133delinsAATC	GRCh38
NC_000002.11:g.26704998_26705001delinsAATC , CM000664.1:g.26704998_26705001delinsAATC	GRCh37
NC_000002.10:g.26558502_26558505delinsAATC	NCBI36
NG_009937.1:g.81566_81569delinsGATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1579+273_1579+276delinsGATT MANE Select	ENSP00000272371.2:n.1579+273_1579+276delinsGATT
ENST00000272371.6:c.1579+273_1579+276delinsGATT	ENSP00000272371.2:n.1579+273_1579+276delinsGATT
ENST00000403946.7:c.1579+273_1579+276delinsGATT	ENSP00000385255.3:n.1579+273_1579+276delinsGATT
NM_001287489.1:c.1579+273_1579+276delinsGATT	NP_001274418.1:n.1579+273_1579+276delinsGATT
NM_194248.2:c.1579+273_1579+276delinsGATT	NP_919224.1:n.1579+273_1579+276delinsGATT
XM_005264644.2:c.1624+273_1624+276delinsGATT	XP_005264701.1:n.1624+273_1624+276delinsGATT
XM_011533185.1:c.1624+273_1624+276delinsGATT	XP_011531487.1:n.1624+273_1624+276delinsGATT
XM_017005338.1:c.1579+273_1579+276delinsGATT	XP_016860827.1:n.1579+273_1579+276delinsGATT
NM_001287489.2:c.1579+273_1579+276delinsGATT	NP_001274418.1:n.1579+273_1579+276delinsGATT
NM_194248.3:c.1579+273_1579+276delinsGATT MANE Select	NP_919224.1:n.1579+273_1579+276delinsGATT