Canonical Allele Identifier: CA1239829252

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482646_26482648delinsCAT , CM000664.2:g.26482646_26482648delinsCAT	GRCh38
NC_000002.11:g.26705514_26705516delinsCAT , CM000664.1:g.26705514_26705516delinsCAT	GRCh37
NC_000002.10:g.26559018_26559020delinsCAT	NCBI36
NG_009937.1:g.81051_81053delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-56_1393-54delinsATG MANE Select	ENSP00000272371.2:n.1393-56_1393-54delinsATG
ENST00000272371.6:c.1393-56_1393-54delinsATG	ENSP00000272371.2:n.1393-56_1393-54delinsATG
ENST00000403946.7:c.1393-56_1393-54delinsATG	ENSP00000385255.3:n.1393-56_1393-54delinsATG
NM_001287489.1:c.1393-56_1393-54delinsATG	NP_001274418.1:n.1393-56_1393-54delinsATG
NM_194248.2:c.1393-56_1393-54delinsATG	NP_919224.1:n.1393-56_1393-54delinsATG
XM_005264644.2:c.1438-56_1438-54delinsATG	XP_005264701.1:n.1438-56_1438-54delinsATG
XM_011533185.1:c.1438-56_1438-54delinsATG	XP_011531487.1:n.1438-56_1438-54delinsATG
XM_017005338.1:c.1393-56_1393-54delinsATG	XP_016860827.1:n.1393-56_1393-54delinsATG
NM_001287489.2:c.1393-56_1393-54delinsATG	NP_001274418.1:n.1393-56_1393-54delinsATG
NM_194248.3:c.1393-56_1393-54delinsATG MANE Select	NP_919224.1:n.1393-56_1393-54delinsATG