Canonical Allele Identifier: CA2042165230

Gene: TBK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64466750_64466752delinsATT , CM000674.2:g.64466750_64466752delinsATT	GRCh38
NC_000012.11:g.64860530_64860532delinsATT , CM000674.1:g.64860530_64860532delinsATT	GRCh37
NC_000012.10:g.63146797_63146799delinsATT	NCBI36
NG_046906.1:g.19691_19693delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331710.10:c.359-151_359-149delinsATT MANE Select	ENSP00000329967.5:n.359-151_359-149delinsATT
ENST00000650708.1:c.235-151_235-149delinsATT
ENST00000650762.1:c.203-151_203-149delinsATT	ENSP00000498758.1:n.203-151_203-149delinsATT
ENST00000650786.1:c.*504-151_*504-149delinsATT	ENSP00000498280.1:n.*504-151_*504-149delinsATT
ENST00000650790.1:c.359-151_359-149delinsATT	ENSP00000498995.1:n.359-151_359-149delinsATT
ENST00000650997.1:c.359-151_359-149delinsATT	ENSP00000498341.1:n.359-151_359-149delinsATT
ENST00000651014.1:c.203-151_203-149delinsATT	ENSP00000498885.1:n.203-151_203-149delinsATT
ENST00000651262.1:c.359-151_359-149delinsATT	ENSP00000498461.1:n.359-151_359-149delinsATT
ENST00000651878.1:c.359-151_359-149delinsATT	ENSP00000499077.1:n.359-151_359-149delinsATT
ENST00000651889.1:n.110-151_110-149delinsATT
ENST00000651947.1:n.447-151_447-149delinsATT
ENST00000652389.1:c.359-151_359-149delinsATT	ENSP00000498414.1:n.359-151_359-149delinsATT
ENST00000652537.1:c.359-151_359-149delinsATT	ENSP00000499102.1:n.359-151_359-149delinsATT
ENST00000652657.1:c.359-151_359-149delinsATT	ENSP00000498887.1:n.359-151_359-149delinsATT
ENST00000676551.1:n.458-151_458-149delinsATT
ENST00000676654.1:n.488-151_488-149delinsATT
ENST00000676684.1:n.488-151_488-149delinsATT
ENST00000676809.1:c.359-151_359-149delinsATT	ENSP00000504298.1:n.359-151_359-149delinsATT
ENST00000676912.1:c.203-151_203-149delinsATT	ENSP00000503567.1:n.203-151_203-149delinsATT
ENST00000676930.1:c.359-151_359-149delinsATT	ENSP00000502899.1:n.359-151_359-149delinsATT
ENST00000677499.1:c.359-151_359-149delinsATT	ENSP00000502875.1:n.359-151_359-149delinsATT
ENST00000677549.1:n.421-151_421-149delinsATT
ENST00000677632.1:c.359-151_359-149delinsATT	ENSP00000504586.1:n.359-151_359-149delinsATT
ENST00000677641.1:c.359-151_359-149delinsATT	ENSP00000504637.1:n.359-151_359-149delinsATT
ENST00000677686.1:n.462-151_462-149delinsATT
ENST00000677759.1:c.216-151_216-149delinsATT	ENSP00000503847.1:n.216-151_216-149delinsATT
ENST00000677831.1:c.359-151_359-149delinsATT	ENSP00000503760.1:n.359-151_359-149delinsATT
ENST00000678079.1:c.131-229_131-227delinsATT	ENSP00000503613.1:n.131-229_131-227delinsATT
ENST00000678180.1:c.359-151_359-149delinsATT	ENSP00000504132.1:n.359-151_359-149delinsATT
ENST00000678197.1:n.343-151_343-149delinsATT
ENST00000679050.1:c.321-151_321-149delinsATT	ENSP00000503595.1:n.321-151_321-149delinsATT
ENST00000679302.1:c.127-151_127-149delinsATT	ENSP00000503553.1:n.127-151_127-149delinsATT
ENST00000331710.9:c.359-151_359-149delinsATT	ENSP00000329967.5:n.359-151_359-149delinsATT
NM_013254.3:c.359-151_359-149delinsATT	NP_037386.1:n.359-151_359-149delinsATT
XM_005268809.1:c.359-151_359-149delinsATT	XP_005268866.1:n.359-151_359-149delinsATT
XM_005268810.1:c.359-151_359-149delinsATT	XP_005268867.1:n.359-151_359-149delinsATT
XR_944524.1:n.518-151_518-149delinsATT
XR_944525.1:n.518-151_518-149delinsATT
XR_001748674.2:n.473-151_473-149delinsATT
NM_013254.4:c.359-151_359-149delinsATT MANE Select	NP_037386.1:n.359-151_359-149delinsATT