Canonical Allele Identifier: CA2559264310

Gene: TBK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64466823_64466824insGTTT , CM000674.2:g.64466823_64466824insGTTT	GRCh38
NC_000012.11:g.64860603_64860604insGTTT , CM000674.1:g.64860603_64860604insGTTT	GRCh37
NC_000012.10:g.63146870_63146871insGTTT	NCBI36
NG_046906.1:g.19764_19765insGTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000331710.10:c.359-78_359-77insGTTT MANE Select	ENSP00000329967.5:n.359-78_359-77insGTTT
ENST00000650708.1:c.235-78_235-77insGTTT
ENST00000650762.1:c.203-78_203-77insGTTT	ENSP00000498758.1:n.203-78_203-77insGTTT
ENST00000650786.1:c.*504-78_*504-77insGTTT	ENSP00000498280.1:n.*504-78_*504-77insGTT...
ENST00000650790.1:c.359-78_359-77insGTTT	ENSP00000498995.1:n.359-78_359-77insGTTT
ENST00000650997.1:c.359-78_359-77insGTTT	ENSP00000498341.1:n.359-78_359-77insGTTT
ENST00000651014.1:c.203-78_203-77insGTTT	ENSP00000498885.1:n.203-78_203-77insGTTT
ENST00000651262.1:c.359-78_359-77insGTTT	ENSP00000498461.1:n.359-78_359-77insGTTT
ENST00000651878.1:c.359-78_359-77insGTTT	ENSP00000499077.1:n.359-78_359-77insGTTT
ENST00000651889.1:n.110-78_110-77insGTTT
ENST00000651947.1:n.447-78_447-77insGTTT
ENST00000652389.1:c.359-78_359-77insGTTT	ENSP00000498414.1:n.359-78_359-77insGTTT
ENST00000652537.1:c.359-78_359-77insGTTT	ENSP00000499102.1:n.359-78_359-77insGTTT
ENST00000652657.1:c.359-78_359-77insGTTT	ENSP00000498887.1:n.359-78_359-77insGTTT
ENST00000676551.1:n.458-78_458-77insGTTT
ENST00000676654.1:n.488-78_488-77insGTTT
ENST00000676684.1:n.488-78_488-77insGTTT
ENST00000676809.1:c.359-78_359-77insGTTT	ENSP00000504298.1:n.359-78_359-77insGTTT
ENST00000676912.1:c.203-78_203-77insGTTT	ENSP00000503567.1:n.203-78_203-77insGTTT
ENST00000676930.1:c.359-78_359-77insGTTT	ENSP00000502899.1:n.359-78_359-77insGTTT
ENST00000677499.1:c.359-78_359-77insGTTT	ENSP00000502875.1:n.359-78_359-77insGTTT
ENST00000677549.1:n.421-78_421-77insGTTT
ENST00000677632.1:c.359-78_359-77insGTTT	ENSP00000504586.1:n.359-78_359-77insGTTT
ENST00000677641.1:c.359-78_359-77insGTTT	ENSP00000504637.1:n.359-78_359-77insGTTT
ENST00000677686.1:n.462-78_462-77insGTTT
ENST00000677759.1:c.216-78_216-77insGTTT	ENSP00000503847.1:n.216-78_216-77insGTTT
ENST00000677831.1:c.359-78_359-77insGTTT	ENSP00000503760.1:n.359-78_359-77insGTTT
ENST00000678079.1:c.131-156_131-155insGTTT	ENSP00000503613.1:n.131-156_131-155insGTT...
ENST00000678180.1:c.359-78_359-77insGTTT	ENSP00000504132.1:n.359-78_359-77insGTTT
ENST00000678197.1:n.343-78_343-77insGTTT
ENST00000679050.1:c.321-78_321-77insGTTT	ENSP00000503595.1:n.321-78_321-77insGTTT
ENST00000679302.1:c.127-78_127-77insGTTT	ENSP00000503553.1:n.127-78_127-77insGTTT
ENST00000331710.9:c.359-78_359-77insGTTT	ENSP00000329967.5:n.359-78_359-77insGTTT
NM_013254.3:c.359-78_359-77insGTTT	NP_037386.1:n.359-78_359-77insGTTT
XM_005268809.1:c.359-78_359-77insGTTT	XP_005268866.1:n.359-78_359-77insGTTT
XM_005268810.1:c.359-78_359-77insGTTT	XP_005268867.1:n.359-78_359-77insGTTT
XR_944524.1:n.518-78_518-77insGTTT
XR_944525.1:n.518-78_518-77insGTTT
XR_001748674.2:n.473-78_473-77insGTTT
NM_013254.4:c.359-78_359-77insGTTT MANE Select	NP_037386.1:n.359-78_359-77insGTTT