Canonical Allele Identifier: CA1239828645

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482133_26482136delinsCATT , CM000664.2:g.26482133_26482136delinsCATT	GRCh38
NC_000002.11:g.26705001_26705004delinsCATT , CM000664.1:g.26705001_26705004delinsCATT	GRCh37
NC_000002.10:g.26558505_26558508delinsCATT	NCBI36
NG_009937.1:g.81563_81566delinsAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1579+270_1579+273delinsAATG MANE Select	ENSP00000272371.2:n.1579+270_1579+273delinsAATG
ENST00000272371.6:c.1579+270_1579+273delinsAATG	ENSP00000272371.2:n.1579+270_1579+273delinsAATG
ENST00000403946.7:c.1579+270_1579+273delinsAATG	ENSP00000385255.3:n.1579+270_1579+273delinsAATG
NM_001287489.1:c.1579+270_1579+273delinsAATG	NP_001274418.1:n.1579+270_1579+273delinsAATG
NM_194248.2:c.1579+270_1579+273delinsAATG	NP_919224.1:n.1579+270_1579+273delinsAATG
XM_005264644.2:c.1624+270_1624+273delinsAATG	XP_005264701.1:n.1624+270_1624+273delinsAATG
XM_011533185.1:c.1624+270_1624+273delinsAATG	XP_011531487.1:n.1624+270_1624+273delinsAATG
XM_017005338.1:c.1579+270_1579+273delinsAATG	XP_016860827.1:n.1579+270_1579+273delinsAATG
NM_001287489.2:c.1579+270_1579+273delinsAATG	NP_001274418.1:n.1579+270_1579+273delinsAATG
NM_194248.3:c.1579+270_1579+273delinsAATG MANE Select	NP_919224.1:n.1579+270_1579+273delinsAATG