Canonical Allele Identifier: CA1239827727

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26475965_26475987delinsGAGTCCGCTGCTGTCGGCGGCAA , CM000664.2:g.26475965_26475987delinsGAGTCCGCTGCTGTCGGCGGCAA	GRCh38
NC_000002.11:g.26698833_26698855delinsGAGTCCGCTGCTGTCGGCGGCAA , CM000664.1:g.26698833_26698855delinsGAGTCCGCTGCTGTCGGCGGCAA	GRCh37
NC_000002.10:g.26552337_26552359delinsGAGTCCGCTGCTGTCGGCGGCAA	NCBI36
NG_009937.1:g.87712_87734delinsTTGCCGCCGACAGCAGCGGACTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.2918_2940delinsTTGCCGCCGACAGCAGCGGACTC MANE Select	ENSP00000272371.2:p.Phe973=
ENST00000339598.8:c.677_699delinsTTGCCGCCGACAGCAGCGGACTC MANE Plus Clinical	ENSP00000344521.3:p.Phe226=
ENST00000402415.8:c.677_699delinsTTGCCGCCGACAGCAGCGGACTC	ENSP00000383906.4:p.Phe226=
ENST00000272371.6:c.2918_2940delinsTTGCCGCCGACAGCAGCGGACTC	ENSP00000272371.2:p.Phe973=
ENST00000338581.10:c.677_699delinsTTGCCGCCGACAGCAGCGGACTC	ENSP00000345137.6:p.Phe226=
ENST00000339598.7:c.677_699delinsTTGCCGCCGACAGCAGCGGACTC	ENSP00000344521.3:p.Phe226=
ENST00000402415.7:c.848_870delinsTTGCCGCCGACAGCAGCGGACTC	ENSP00000383906.3:p.Phe283=
ENST00000403946.7:c.2918_2940delinsTTGCCGCCGACAGCAGCGGACTC	ENSP00000385255.3:p.Phe973=
NM_001287489.1:c.2918_2940delinsTTGCCGCCGACAGCAGCGGACTC	NP_001274418.1:p.Phe973=
NM_004802.3:c.677_699delinsTTGCCGCCGACAGCAGCGGACTC	NP_004793.2:p.Phe226=
NM_194248.2:c.2918_2940delinsTTGCCGCCGACAGCAGCGGACTC	NP_919224.1:p.Phe973=
NM_194322.2:c.848_870delinsTTGCCGCCGACAGCAGCGGACTC	NP_919303.1:p.Phe283=
NM_194323.2:c.677_699delinsTTGCCGCCGACAGCAGCGGACTC	NP_919304.1:p.Phe226=
XM_005264644.2:c.2963_2985delinsTTGCCGCCGACAGCAGCGGACTC	XP_005264701.1:p.Phe988=
XM_011533185.1:c.2963_2985delinsTTGCCGCCGACAGCAGCGGACTC	XP_011531487.1:p.Phe988=
XM_017005338.1:c.2918_2940delinsTTGCCGCCGACAGCAGCGGACTC	XP_016860827.1:p.Phe973=
NM_001287489.2:c.2918_2940delinsTTGCCGCCGACAGCAGCGGACTC	NP_001274418.1:p.Phe973=
NM_004802.4:c.677_699delinsTTGCCGCCGACAGCAGCGGACTC	NP_004793.2:p.Phe226=
NM_194248.3:c.2918_2940delinsTTGCCGCCGACAGCAGCGGACTC MANE Select	NP_919224.1:p.Phe973=
NM_194322.3:c.848_870delinsTTGCCGCCGACAGCAGCGGACTC	NP_919303.1:p.Phe283=
NM_194323.3:c.677_699delinsTTGCCGCCGACAGCAGCGGACTC MANE Plus Clinical	NP_919304.1:p.Phe226=