Canonical Allele Identifier: CA2575213456

Gene: TBK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64466852_64466853insGTCT , CM000674.2:g.64466852_64466853insGTCT	GRCh38
NC_000012.11:g.64860632_64860633insGTCT , CM000674.1:g.64860632_64860633insGTCT	GRCh37
NC_000012.10:g.63146899_63146900insGTCT	NCBI36
NG_046906.1:g.19793_19794insGTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000331710.10:c.359-49_359-48insGTCT MANE Select	ENSP00000329967.5:n.359-49_359-48insGTCT
ENST00000650708.1:c.235-49_235-48insGTCT
ENST00000650762.1:c.203-49_203-48insGTCT	ENSP00000498758.1:n.203-49_203-48insGTCT
ENST00000650786.1:c.*504-49_*504-48insGTCT	ENSP00000498280.1:n.*504-49_*504-48insGTC...
ENST00000650790.1:c.359-49_359-48insGTCT	ENSP00000498995.1:n.359-49_359-48insGTCT
ENST00000650997.1:c.359-49_359-48insGTCT	ENSP00000498341.1:n.359-49_359-48insGTCT
ENST00000651014.1:c.203-49_203-48insGTCT	ENSP00000498885.1:n.203-49_203-48insGTCT
ENST00000651262.1:c.359-49_359-48insGTCT	ENSP00000498461.1:n.359-49_359-48insGTCT
ENST00000651878.1:c.359-49_359-48insGTCT	ENSP00000499077.1:n.359-49_359-48insGTCT
ENST00000651889.1:n.110-49_110-48insGTCT
ENST00000651947.1:n.447-49_447-48insGTCT
ENST00000652389.1:c.359-49_359-48insGTCT	ENSP00000498414.1:n.359-49_359-48insGTCT
ENST00000652537.1:c.359-49_359-48insGTCT	ENSP00000499102.1:n.359-49_359-48insGTCT
ENST00000652657.1:c.359-49_359-48insGTCT	ENSP00000498887.1:n.359-49_359-48insGTCT
ENST00000676551.1:n.458-49_458-48insGTCT
ENST00000676654.1:n.488-49_488-48insGTCT
ENST00000676684.1:n.488-49_488-48insGTCT
ENST00000676809.1:c.359-49_359-48insGTCT	ENSP00000504298.1:n.359-49_359-48insGTCT
ENST00000676912.1:c.203-49_203-48insGTCT	ENSP00000503567.1:n.203-49_203-48insGTCT
ENST00000676930.1:c.359-49_359-48insGTCT	ENSP00000502899.1:n.359-49_359-48insGTCT
ENST00000677499.1:c.359-49_359-48insGTCT	ENSP00000502875.1:n.359-49_359-48insGTCT
ENST00000677549.1:n.421-49_421-48insGTCT
ENST00000677632.1:c.359-49_359-48insGTCT	ENSP00000504586.1:n.359-49_359-48insGTCT
ENST00000677641.1:c.359-49_359-48insGTCT	ENSP00000504637.1:n.359-49_359-48insGTCT
ENST00000677686.1:n.462-49_462-48insGTCT
ENST00000677759.1:c.216-49_216-48insGTCT	ENSP00000503847.1:n.216-49_216-48insGTCT
ENST00000677831.1:c.359-49_359-48insGTCT	ENSP00000503760.1:n.359-49_359-48insGTCT
ENST00000678079.1:c.131-127_131-126insGTCT	ENSP00000503613.1:n.131-127_131-126insGTC...
ENST00000678180.1:c.359-49_359-48insGTCT	ENSP00000504132.1:n.359-49_359-48insGTCT
ENST00000678197.1:n.343-49_343-48insGTCT
ENST00000679050.1:c.321-49_321-48insGTCT	ENSP00000503595.1:n.321-49_321-48insGTCT
ENST00000679302.1:c.127-49_127-48insGTCT	ENSP00000503553.1:n.127-49_127-48insGTCT
ENST00000331710.9:c.359-49_359-48insGTCT	ENSP00000329967.5:n.359-49_359-48insGTCT
NM_013254.3:c.359-49_359-48insGTCT	NP_037386.1:n.359-49_359-48insGTCT
XM_005268809.1:c.359-49_359-48insGTCT	XP_005268866.1:n.359-49_359-48insGTCT
XM_005268810.1:c.359-49_359-48insGTCT	XP_005268867.1:n.359-49_359-48insGTCT
XR_944524.1:n.518-49_518-48insGTCT
XR_944525.1:n.518-49_518-48insGTCT
XR_001748674.2:n.473-49_473-48insGTCT
NM_013254.4:c.359-49_359-48insGTCT MANE Select	NP_037386.1:n.359-49_359-48insGTCT