Canonical Allele Identifier: CA2576699641

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26480363_26480364insA , CM000664.2:g.26480363_26480364insA	GRCh38
NC_000002.11:g.26703231_26703232insA , CM000664.1:g.26703231_26703232insA	GRCh37
NC_000002.10:g.26556735_26556736insA	NCBI36
NG_009937.1:g.83335_83336insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1804-53_1804-52insT MANE Select	ENSP00000272371.2:n.1804-53_1804-52insT
ENST00000272371.6:c.1804-53_1804-52insT	ENSP00000272371.2:n.1804-53_1804-52insT
ENST00000403946.7:c.1804-53_1804-52insT	ENSP00000385255.3:n.1804-53_1804-52insT
NM_001287489.1:c.1804-53_1804-52insT	NP_001274418.1:n.1804-53_1804-52insT
NM_194248.2:c.1804-53_1804-52insT	NP_919224.1:n.1804-53_1804-52insT
XM_005264644.2:c.1849-53_1849-52insT	XP_005264701.1:n.1849-53_1849-52insT
XM_011533185.1:c.1849-53_1849-52insT	XP_011531487.1:n.1849-53_1849-52insT
XM_017005338.1:c.1804-53_1804-52insT	XP_016860827.1:n.1804-53_1804-52insT
NM_001287489.2:c.1804-53_1804-52insT	NP_001274418.1:n.1804-53_1804-52insT
NM_194248.3:c.1804-53_1804-52insT MANE Select	NP_919224.1:n.1804-53_1804-52insT