Canonical Allele Identifier: CA1239829569

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482859_26482861delinsGCA , CM000664.2:g.26482859_26482861delinsGCA	GRCh38
NC_000002.11:g.26705727_26705729delinsGCA , CM000664.1:g.26705727_26705729delinsGCA	GRCh37
NC_000002.10:g.26559231_26559233delinsGCA	NCBI36
NG_009937.1:g.80838_80840delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-269_1393-267delinsTGC MANE Select	ENSP00000272371.2:n.1393-269_1393-267delinsTGC
ENST00000272371.6:c.1393-269_1393-267delinsTGC	ENSP00000272371.2:n.1393-269_1393-267delinsTGC
ENST00000403946.7:c.1393-269_1393-267delinsTGC	ENSP00000385255.3:n.1393-269_1393-267delinsTGC
NM_001287489.1:c.1393-269_1393-267delinsTGC	NP_001274418.1:n.1393-269_1393-267delinsTGC
NM_194248.2:c.1393-269_1393-267delinsTGC	NP_919224.1:n.1393-269_1393-267delinsTGC
XM_005264644.2:c.1438-269_1438-267delinsTGC	XP_005264701.1:n.1438-269_1438-267delinsTGC
XM_011533185.1:c.1438-269_1438-267delinsTGC	XP_011531487.1:n.1438-269_1438-267delinsTGC
XM_017005338.1:c.1393-269_1393-267delinsTGC	XP_016860827.1:n.1393-269_1393-267delinsTGC
NM_001287489.2:c.1393-269_1393-267delinsTGC	NP_001274418.1:n.1393-269_1393-267delinsTGC
NM_194248.3:c.1393-269_1393-267delinsTGC MANE Select	NP_919224.1:n.1393-269_1393-267delinsTGC