Canonical Allele Identifier: CA1239818385
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26467355_26467356delinsAG , CM000664.2:g.26467355_26467356delinsAG GRCh38
NC_000002.11:g.26690223_26690224delinsAG , CM000664.1:g.26690223_26690224delinsAG GRCh37
NC_000002.10:g.26543727_26543728delinsAG NCBI36
NG_009937.1:g.96343_96344delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.4227+9_4227+10delinsCT MANE Select ENSP00000272371.2:n.4227+9_4227+10delinsCT
ENST00000339598.8:c.1926+9_1926+10delinsCT MANE Plus Clinical ENSP00000344521.3:n.1926+9_1926+10delinsCT
ENST00000402415.8:c.1986+9_1986+10delinsCT ENSP00000383906.4:n.1986+9_1986+10delinsCT
ENST00000272371.6:c.4227+9_4227+10delinsCT ENSP00000272371.2:n.4227+9_4227+10delinsCT
ENST00000338581.10:c.1926+9_1926+10delinsCT ENSP00000345137.6:n.1926+9_1926+10delinsCT
ENST00000339598.7:c.1926+9_1926+10delinsCT ENSP00000344521.3:n.1926+9_1926+10delinsCT
ENST00000402415.7:c.2157+9_2157+10delinsCT ENSP00000383906.3:n.2157+9_2157+10delinsCT
ENST00000403946.7:c.4227+9_4227+10delinsCT ENSP00000385255.3:n.4227+9_4227+10delinsCT
NM_001287489.1:c.4227+9_4227+10delinsCT NP_001274418.1:n.4227+9_4227+10delinsCT
NM_004802.3:c.1926+9_1926+10delinsCT NP_004793.2:n.1926+9_1926+10delinsCT
NM_194248.2:c.4227+9_4227+10delinsCT NP_919224.1:n.4227+9_4227+10delinsCT
NM_194322.2:c.2157+9_2157+10delinsCT NP_919303.1:n.2157+9_2157+10delinsCT
NM_194323.2:c.1926+9_1926+10delinsCT NP_919304.1:n.1926+9_1926+10delinsCT
XM_005264644.2:c.4212+9_4212+10delinsCT XP_005264701.1:n.4212+9_4212+10delinsCT
XM_011533185.1:c.4272+9_4272+10delinsCT XP_011531487.1:n.4272+9_4272+10delinsCT
XM_017005338.1:c.4167+9_4167+10delinsCT XP_016860827.1:n.4167+9_4167+10delinsCT
NM_001287489.2:c.4227+9_4227+10delinsCT NP_001274418.1:n.4227+9_4227+10delinsCT
NM_004802.4:c.1926+9_1926+10delinsCT NP_004793.2:n.1926+9_1926+10delinsCT
NM_194248.3:c.4227+9_4227+10delinsCT MANE Select NP_919224.1:n.4227+9_4227+10delinsCT
NM_194322.3:c.2157+9_2157+10delinsCT NP_919303.1:n.2157+9_2157+10delinsCT
NM_194323.3:c.1926+9_1926+10delinsCT MANE Plus Clinical NP_919304.1:n.1926+9_1926+10delinsCT