Canonical Allele Identifier: CA1239829402

Gene: OTOF

Linked Data

• dbSNP Id: rs1665580714

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482753_26482754insCACA , CM000664.2:g.26482753_26482754insCACA	GRCh38
NC_000002.11:g.26705621_26705622insCACA , CM000664.1:g.26705621_26705622insCACA	GRCh37
NC_000002.10:g.26559125_26559126insCACA	NCBI36
NG_009937.1:g.80945_80946insTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-162_1393-161insTGTG MANE Select	ENSP00000272371.2:n.1393-162_1393-161insTGTG
ENST00000272371.6:c.1393-162_1393-161insTGTG	ENSP00000272371.2:n.1393-162_1393-161insTGTG
ENST00000403946.7:c.1393-162_1393-161insTGTG	ENSP00000385255.3:n.1393-162_1393-161insTGTG
NM_001287489.1:c.1393-162_1393-161insTGTG	NP_001274418.1:n.1393-162_1393-161insTGTG
NM_194248.2:c.1393-162_1393-161insTGTG	NP_919224.1:n.1393-162_1393-161insTGTG
XM_005264644.2:c.1438-162_1438-161insTGTG	XP_005264701.1:n.1438-162_1438-161insTGTG
XM_011533185.1:c.1438-162_1438-161insTGTG	XP_011531487.1:n.1438-162_1438-161insTGTG
XM_017005338.1:c.1393-162_1393-161insTGTG	XP_016860827.1:n.1393-162_1393-161insTGTG
NM_001287489.2:c.1393-162_1393-161insTGTG	NP_001274418.1:n.1393-162_1393-161insTGTG
NM_194248.3:c.1393-162_1393-161insTGTG MANE Select	NP_919224.1:n.1393-162_1393-161insTGTG