Canonical Allele Identifier: CA1239829381

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482742_26482744delinsTGC , CM000664.2:g.26482742_26482744delinsTGC	GRCh38
NC_000002.11:g.26705610_26705612delinsTGC , CM000664.1:g.26705610_26705612delinsTGC	GRCh37
NC_000002.10:g.26559114_26559116delinsTGC	NCBI36
NG_009937.1:g.80955_80957delinsGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-152_1393-150delinsGCA MANE Select	ENSP00000272371.2:n.1393-152_1393-150delinsGCA
ENST00000272371.6:c.1393-152_1393-150delinsGCA	ENSP00000272371.2:n.1393-152_1393-150delinsGCA
ENST00000403946.7:c.1393-152_1393-150delinsGCA	ENSP00000385255.3:n.1393-152_1393-150delinsGCA
NM_001287489.1:c.1393-152_1393-150delinsGCA	NP_001274418.1:n.1393-152_1393-150delinsGCA
NM_194248.2:c.1393-152_1393-150delinsGCA	NP_919224.1:n.1393-152_1393-150delinsGCA
XM_005264644.2:c.1438-152_1438-150delinsGCA	XP_005264701.1:n.1438-152_1438-150delinsGCA
XM_011533185.1:c.1438-152_1438-150delinsGCA	XP_011531487.1:n.1438-152_1438-150delinsGCA
XM_017005338.1:c.1393-152_1393-150delinsGCA	XP_016860827.1:n.1393-152_1393-150delinsGCA
NM_001287489.2:c.1393-152_1393-150delinsGCA	NP_001274418.1:n.1393-152_1393-150delinsGCA
NM_194248.3:c.1393-152_1393-150delinsGCA MANE Select	NP_919224.1:n.1393-152_1393-150delinsGCA