Canonical Allele Identifier: CA1239830695

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483942_26483943delinsAT , CM000664.2:g.26483942_26483943delinsAT	GRCh38
NC_000002.11:g.26706810_26706811delinsAT , CM000664.1:g.26706810_26706811delinsAT	GRCh37
NC_000002.10:g.26560314_26560315delinsAT	NCBI36
NG_009937.1:g.79756_79757delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1206-295_1206-294delinsAT MANE Select	ENSP00000272371.2:n.1206-295_1206-294delinsAT
ENST00000272371.6:c.1206-295_1206-294delinsAT	ENSP00000272371.2:n.1206-295_1206-294delinsAT
ENST00000403946.7:c.1206-295_1206-294delinsAT	ENSP00000385255.3:n.1206-295_1206-294delinsAT
NM_001287489.1:c.1206-295_1206-294delinsAT	NP_001274418.1:n.1206-295_1206-294delinsAT
NM_194248.2:c.1206-295_1206-294delinsAT	NP_919224.1:n.1206-295_1206-294delinsAT
XM_005264644.2:c.1251-295_1251-294delinsAT	XP_005264701.1:n.1251-295_1251-294delinsAT
XM_011533185.1:c.1251-295_1251-294delinsAT	XP_011531487.1:n.1251-295_1251-294delinsAT
XM_017005338.1:c.1206-295_1206-294delinsAT	XP_016860827.1:n.1206-295_1206-294delinsAT
NM_001287489.2:c.1206-295_1206-294delinsAT	NP_001274418.1:n.1206-295_1206-294delinsAT
NM_194248.3:c.1206-295_1206-294delinsAT MANE Select	NP_919224.1:n.1206-295_1206-294delinsAT