Canonical Allele Identifier: CA1239818501
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26467437_26467440delinsTTTC , CM000664.2:g.26467437_26467440delinsTTTC GRCh38
NC_000002.11:g.26690305_26690308delinsTTTC , CM000664.1:g.26690305_26690308delinsTTTC GRCh37
NC_000002.10:g.26543809_26543812delinsTTTC NCBI36
NG_009937.1:g.96259_96262delinsGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.4152_4155delinsGAAA MANE Select ENSP00000272371.2:p.Lys1384=
ENST00000339598.8:c.1851_1854delinsGAAA MANE Plus Clinical ENSP00000344521.3:p.Lys617=
ENST00000402415.8:c.1911_1914delinsGAAA ENSP00000383906.4:p.Lys637=
ENST00000272371.6:c.4152_4155delinsGAAA ENSP00000272371.2:p.Lys1384=
ENST00000338581.10:c.1851_1854delinsGAAA ENSP00000345137.6:p.Lys617=
ENST00000339598.7:c.1851_1854delinsGAAA ENSP00000344521.3:p.Lys617=
ENST00000402415.7:c.2082_2085delinsGAAA ENSP00000383906.3:p.Lys694=
ENST00000403946.7:c.4152_4155delinsGAAA ENSP00000385255.3:p.Lys1384=
NM_001287489.1:c.4152_4155delinsGAAA NP_001274418.1:p.Lys1384=
NM_004802.3:c.1851_1854delinsGAAA NP_004793.2:p.Lys617=
NM_194248.2:c.4152_4155delinsGAAA NP_919224.1:p.Lys1384=
NM_194322.2:c.2082_2085delinsGAAA NP_919303.1:p.Lys694=
NM_194323.2:c.1851_1854delinsGAAA NP_919304.1:p.Lys617=
XM_005264644.2:c.4137_4140delinsGAAA XP_005264701.1:p.Lys1379=
XM_011533185.1:c.4197_4200delinsGAAA XP_011531487.1:p.Lys1399=
XM_017005338.1:c.4092_4095delinsGAAA XP_016860827.1:p.Lys1364=
NM_001287489.2:c.4152_4155delinsGAAA NP_001274418.1:p.Lys1384=
NM_004802.4:c.1851_1854delinsGAAA NP_004793.2:p.Lys617=
NM_194248.3:c.4152_4155delinsGAAA MANE Select NP_919224.1:p.Lys1384=
NM_194322.3:c.2082_2085delinsGAAA NP_919303.1:p.Lys694=
NM_194323.3:c.1851_1854delinsGAAA MANE Plus Clinical NP_919304.1:p.Lys617=