Canonical Allele Identifier: CA1239824035

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460110_26460112delinsAAC , CM000664.2:g.26460110_26460112delinsAAC	GRCh38
NC_000002.11:g.26682978_26682980delinsAAC , CM000664.1:g.26682978_26682980delinsAAC	GRCh37
NC_000002.10:g.26536482_26536484delinsAAC	NCBI36
NG_009937.1:g.103587_103589delinsGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5907_5909delinsGTT MANE Select	ENSP00000272371.2:p.Leu1969=
ENST00000339598.8:c.3512+535_3512+537delinsGTT MANE Plus Clinical	ENSP00000344521.3:n.3512+535_3512+537deli...
ENST00000402415.8:c.3666_3668delinsGTT	ENSP00000383906.4:p.Leu1222=
ENST00000272371.6:c.5907_5909delinsGTT	ENSP00000272371.2:p.Leu1969=
ENST00000338581.10:c.3606_3608delinsGTT	ENSP00000345137.6:p.Leu1202=
ENST00000339598.7:c.3512+535_3512+537delinsGTT	ENSP00000344521.3:n.3512+535_3512+537deli...
ENST00000402415.7:c.3837_3839delinsGTT	ENSP00000383906.3:p.Leu1279=
ENST00000403946.7:c.5813+535_5813+537delinsGTT	ENSP00000385255.3:n.5813+535_5813+537deli...
NM_001287489.1:c.5813+535_5813+537delinsGTT	NP_001274418.1:n.5813+535_5813+537delinsG...
NM_004802.3:c.3606_3608delinsGTT	NP_004793.2:p.Leu1202=
NM_194248.2:c.5907_5909delinsGTT	NP_919224.1:p.Leu1969=
NM_194322.2:c.3837_3839delinsGTT	NP_919303.1:p.Leu1279=
NM_194323.2:c.3512+535_3512+537delinsGTT	NP_919304.1:n.3512+535_3512+537delinsGTT
XM_005264644.2:c.5798+535_5798+537delinsGTT	XP_005264701.1:n.5798+535_5798+537delinsG...
XM_011533185.1:c.5858+535_5858+537delinsGTT	XP_011531487.1:n.5858+535_5858+537delinsG...
XM_017005338.1:c.5847_5849delinsGTT	XP_016860827.1:p.Leu1949=
NM_001287489.2:c.5813+535_5813+537delinsGTT	NP_001274418.1:n.5813+535_5813+537delinsG...
NM_004802.4:c.3606_3608delinsGTT	NP_004793.2:p.Leu1202=
NM_194248.3:c.5907_5909delinsGTT MANE Select	NP_919224.1:p.Leu1969=
NM_194322.3:c.3837_3839delinsGTT	NP_919303.1:p.Leu1279=
NM_194323.3:c.3512+535_3512+537delinsGTT MANE Plus Clinical	NP_919304.1:n.3512+535_3512+537delinsGTT