Canonical Allele Identifier: CA1239818001

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467196_26467199delinsAAGT , CM000664.2:g.26467196_26467199delinsAAGT	GRCh38
NC_000002.11:g.26690064_26690067delinsAAGT , CM000664.1:g.26690064_26690067delinsAAGT	GRCh37
NC_000002.10:g.26543568_26543571delinsAAGT	NCBI36
NG_009937.1:g.96500_96503delinsACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4262_4265delinsACTT MANE Select	ENSP00000272371.2:p.Asn1421=
ENST00000339598.8:c.1961_1964delinsACTT MANE Plus Clinical	ENSP00000344521.3:p.Asn654=
ENST00000402415.8:c.2021_2024delinsACTT	ENSP00000383906.4:p.Asn674=
ENST00000272371.6:c.4262_4265delinsACTT	ENSP00000272371.2:p.Asn1421=
ENST00000338581.10:c.1961_1964delinsACTT	ENSP00000345137.6:p.Asn654=
ENST00000339598.7:c.1961_1964delinsACTT	ENSP00000344521.3:p.Asn654=
ENST00000402415.7:c.2192_2195delinsACTT	ENSP00000383906.3:p.Asn731=
ENST00000403946.7:c.4262_4265delinsACTT	ENSP00000385255.3:p.Asn1421=
NM_001287489.1:c.4262_4265delinsACTT	NP_001274418.1:p.Asn1421=
NM_004802.3:c.1961_1964delinsACTT	NP_004793.2:p.Asn654=
NM_194248.2:c.4262_4265delinsACTT	NP_919224.1:p.Asn1421=
NM_194322.2:c.2192_2195delinsACTT	NP_919303.1:p.Asn731=
NM_194323.2:c.1961_1964delinsACTT	NP_919304.1:p.Asn654=
XM_005264644.2:c.4247_4250delinsACTT	XP_005264701.1:p.Asn1416=
XM_011533185.1:c.4307_4310delinsACTT	XP_011531487.1:p.Asn1436=
XM_017005338.1:c.4202_4205delinsACTT	XP_016860827.1:p.Asn1401=
NM_001287489.2:c.4262_4265delinsACTT	NP_001274418.1:p.Asn1421=
NM_004802.4:c.1961_1964delinsACTT	NP_004793.2:p.Asn654=
NM_194248.3:c.4262_4265delinsACTT MANE Select	NP_919224.1:p.Asn1421=
NM_194322.3:c.2192_2195delinsACTT	NP_919303.1:p.Asn731=
NM_194323.3:c.1961_1964delinsACTT MANE Plus Clinical	NP_919304.1:p.Asn654=