Canonical Allele Identifier: CA1239827422

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26480500_26480501delinsCA , CM000664.2:g.26480500_26480501delinsCA	GRCh38
NC_000002.11:g.26703368_26703369delinsCA , CM000664.1:g.26703368_26703369delinsCA	GRCh37
NC_000002.10:g.26556872_26556873delinsCA	NCBI36
NG_009937.1:g.83198_83199delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1804-190_1804-189delinsTG MANE Select	ENSP00000272371.2:n.1804-190_1804-189delinsTG
ENST00000272371.6:c.1804-190_1804-189delinsTG	ENSP00000272371.2:n.1804-190_1804-189delinsTG
ENST00000403946.7:c.1804-190_1804-189delinsTG	ENSP00000385255.3:n.1804-190_1804-189delinsTG
NM_001287489.1:c.1804-190_1804-189delinsTG	NP_001274418.1:n.1804-190_1804-189delinsTG
NM_194248.2:c.1804-190_1804-189delinsTG	NP_919224.1:n.1804-190_1804-189delinsTG
XM_005264644.2:c.1849-190_1849-189delinsTG	XP_005264701.1:n.1849-190_1849-189delinsTG
XM_011533185.1:c.1849-190_1849-189delinsTG	XP_011531487.1:n.1849-190_1849-189delinsTG
XM_017005338.1:c.1804-190_1804-189delinsTG	XP_016860827.1:n.1804-190_1804-189delinsTG
NM_001287489.2:c.1804-190_1804-189delinsTG	NP_001274418.1:n.1804-190_1804-189delinsTG
NM_194248.3:c.1804-190_1804-189delinsTG MANE Select	NP_919224.1:n.1804-190_1804-189delinsTG