Canonical Allele Identifier: CA1239829555

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482856_26482857delinsGA , CM000664.2:g.26482856_26482857delinsGA	GRCh38
NC_000002.11:g.26705724_26705725delinsGA , CM000664.1:g.26705724_26705725delinsGA	GRCh37
NC_000002.10:g.26559228_26559229delinsGA	NCBI36
NG_009937.1:g.80842_80843delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-265_1393-264delinsTC MANE Select	ENSP00000272371.2:n.1393-265_1393-264delinsTC
ENST00000272371.6:c.1393-265_1393-264delinsTC	ENSP00000272371.2:n.1393-265_1393-264delinsTC
ENST00000403946.7:c.1393-265_1393-264delinsTC	ENSP00000385255.3:n.1393-265_1393-264delinsTC
NM_001287489.1:c.1393-265_1393-264delinsTC	NP_001274418.1:n.1393-265_1393-264delinsTC
NM_194248.2:c.1393-265_1393-264delinsTC	NP_919224.1:n.1393-265_1393-264delinsTC
XM_005264644.2:c.1438-265_1438-264delinsTC	XP_005264701.1:n.1438-265_1438-264delinsTC
XM_011533185.1:c.1438-265_1438-264delinsTC	XP_011531487.1:n.1438-265_1438-264delinsTC
XM_017005338.1:c.1393-265_1393-264delinsTC	XP_016860827.1:n.1393-265_1393-264delinsTC
NM_001287489.2:c.1393-265_1393-264delinsTC	NP_001274418.1:n.1393-265_1393-264delinsTC
NM_194248.3:c.1393-265_1393-264delinsTC MANE Select	NP_919224.1:n.1393-265_1393-264delinsTC