Canonical Allele Identifier: CA2658234866

Gene: OTOF

Linked Data

• gnomAD v4: 2-26467385-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467386_26467388dup , CM000664.2:g.26467386_26467388dup	GRCh38
NC_000002.11:g.26690254_26690256dup , CM000664.1:g.26690254_26690256dup	GRCh37
NC_000002.10:g.26543758_26543760dup	NCBI36
NG_009937.1:g.96311_96313dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4204_4206dup MANE Select	ENSP00000272371.2:p.Lys1402_Pro1403insLys
ENST00000339598.8:c.1903_1905dup MANE Plus Clinical	ENSP00000344521.3:p.Lys635_Pro636insLys
ENST00000402415.8:c.1963_1965dup	ENSP00000383906.4:p.Lys655_Pro656insLys
ENST00000272371.6:c.4204_4206dup	ENSP00000272371.2:p.Lys1402_Pro1403insLys
ENST00000338581.10:c.1903_1905dup	ENSP00000345137.6:p.Lys635_Pro636insLys
ENST00000339598.7:c.1903_1905dup	ENSP00000344521.3:p.Lys635_Pro636insLys
ENST00000402415.7:c.2134_2136dup	ENSP00000383906.3:p.Lys712_Pro713insLys
ENST00000403946.7:c.4204_4206dup	ENSP00000385255.3:p.Lys1402_Pro1403insLys
NM_001287489.1:c.4204_4206dup	NP_001274418.1:p.Lys1402_Pro1403insLys
NM_004802.3:c.1903_1905dup	NP_004793.2:p.Lys635_Pro636insLys
NM_194248.2:c.4204_4206dup	NP_919224.1:p.Lys1402_Pro1403insLys
NM_194322.2:c.2134_2136dup	NP_919303.1:p.Lys712_Pro713insLys
NM_194323.2:c.1903_1905dup	NP_919304.1:p.Lys635_Pro636insLys
XM_005264644.2:c.4189_4191dup	XP_005264701.1:p.Lys1397_Pro1398insLys
XM_011533185.1:c.4249_4251dup	XP_011531487.1:p.Lys1417_Pro1418insLys
XM_017005338.1:c.4144_4146dup	XP_016860827.1:p.Lys1382_Pro1383insLys
NM_001287489.2:c.4204_4206dup	NP_001274418.1:p.Lys1402_Pro1403insLys
NM_004802.4:c.1903_1905dup	NP_004793.2:p.Lys635_Pro636insLys
NM_194248.3:c.4204_4206dup MANE Select	NP_919224.1:p.Lys1402_Pro1403insLys
NM_194322.3:c.2134_2136dup	NP_919303.1:p.Lys712_Pro713insLys
NM_194323.3:c.1903_1905dup MANE Plus Clinical	NP_919304.1:p.Lys635_Pro636insLys