Canonical Allele Identifier: CA1239829333

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482714_26482720delinsTGCATGC , CM000664.2:g.26482714_26482720delinsTGCATGC	GRCh38
NC_000002.11:g.26705582_26705588delinsTGCATGC , CM000664.1:g.26705582_26705588delinsTGCATGC	GRCh37
NC_000002.10:g.26559086_26559092delinsTGCATGC	NCBI36
NG_009937.1:g.80979_80985delinsGCATGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-128_1393-122delinsGCATGCA MANE Select	ENSP00000272371.2:n.1393-128_1393-122delinsGCATGCA
ENST00000272371.6:c.1393-128_1393-122delinsGCATGCA	ENSP00000272371.2:n.1393-128_1393-122delinsGCATGCA
ENST00000403946.7:c.1393-128_1393-122delinsGCATGCA	ENSP00000385255.3:n.1393-128_1393-122delinsGCATGCA
NM_001287489.1:c.1393-128_1393-122delinsGCATGCA	NP_001274418.1:n.1393-128_1393-122delinsGCATGCA
NM_194248.2:c.1393-128_1393-122delinsGCATGCA	NP_919224.1:n.1393-128_1393-122delinsGCATGCA
XM_005264644.2:c.1438-128_1438-122delinsGCATGCA	XP_005264701.1:n.1438-128_1438-122delinsGCATGCA
XM_011533185.1:c.1438-128_1438-122delinsGCATGCA	XP_011531487.1:n.1438-128_1438-122delinsGCATGCA
XM_017005338.1:c.1393-128_1393-122delinsGCATGCA	XP_016860827.1:n.1393-128_1393-122delinsGCATGCA
NM_001287489.2:c.1393-128_1393-122delinsGCATGCA	NP_001274418.1:n.1393-128_1393-122delinsGCATGCA
NM_194248.3:c.1393-128_1393-122delinsGCATGCA MANE Select	NP_919224.1:n.1393-128_1393-122delinsGCATGCA