Canonical Allele Identifier: CA1239829342

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482720_26482724delinsCGTGT , CM000664.2:g.26482720_26482724delinsCGTGT	GRCh38
NC_000002.11:g.26705588_26705592delinsCGTGT , CM000664.1:g.26705588_26705592delinsCGTGT	GRCh37
NC_000002.10:g.26559092_26559096delinsCGTGT	NCBI36
NG_009937.1:g.80975_80979delinsACACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-132_1393-128delinsACACG MANE Select	ENSP00000272371.2:n.1393-132_1393-128delinsACACG
ENST00000272371.6:c.1393-132_1393-128delinsACACG	ENSP00000272371.2:n.1393-132_1393-128delinsACACG
ENST00000403946.7:c.1393-132_1393-128delinsACACG	ENSP00000385255.3:n.1393-132_1393-128delinsACACG
NM_001287489.1:c.1393-132_1393-128delinsACACG	NP_001274418.1:n.1393-132_1393-128delinsACACG
NM_194248.2:c.1393-132_1393-128delinsACACG	NP_919224.1:n.1393-132_1393-128delinsACACG
XM_005264644.2:c.1438-132_1438-128delinsACACG	XP_005264701.1:n.1438-132_1438-128delinsACACG
XM_011533185.1:c.1438-132_1438-128delinsACACG	XP_011531487.1:n.1438-132_1438-128delinsACACG
XM_017005338.1:c.1393-132_1393-128delinsACACG	XP_016860827.1:n.1393-132_1393-128delinsACACG
NM_001287489.2:c.1393-132_1393-128delinsACACG	NP_001274418.1:n.1393-132_1393-128delinsACACG
NM_194248.3:c.1393-132_1393-128delinsACACG MANE Select	NP_919224.1:n.1393-132_1393-128delinsACACG