Canonical Allele Identifier: CA2548268806

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482745_26482760dup , CM000664.2:g.26482745_26482760dup	GRCh38
NC_000002.11:g.26705613_26705628dup , CM000664.1:g.26705613_26705628dup	GRCh37
NC_000002.10:g.26559117_26559132dup	NCBI36
NG_009937.1:g.80943_80958dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-164_1393-149dup MANE Select	ENSP00000272371.2:n.1393-164_1393-149dup
ENST00000272371.6:c.1393-164_1393-149dup	ENSP00000272371.2:n.1393-164_1393-149dup
ENST00000403946.7:c.1393-164_1393-149dup	ENSP00000385255.3:n.1393-164_1393-149dup
NM_001287489.1:c.1393-164_1393-149dup	NP_001274418.1:n.1393-164_1393-149dup
NM_194248.2:c.1393-164_1393-149dup	NP_919224.1:n.1393-164_1393-149dup
XM_005264644.2:c.1438-164_1438-149dup	XP_005264701.1:n.1438-164_1438-149dup
XM_011533185.1:c.1438-164_1438-149dup	XP_011531487.1:n.1438-164_1438-149dup
XM_017005338.1:c.1393-164_1393-149dup	XP_016860827.1:n.1393-164_1393-149dup
NM_001287489.2:c.1393-164_1393-149dup	NP_001274418.1:n.1393-164_1393-149dup
NM_194248.3:c.1393-164_1393-149dup MANE Select	NP_919224.1:n.1393-164_1393-149dup