Canonical Allele Identifier: CA6669005

Gene: TBK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64485472C>T , CM000674.2:g.64485472C>T	GRCh38
NC_000012.11:g.64879252C>T , CM000674.1:g.64879252C>T	GRCh37
NC_000012.10:g.63165519C>T	NCBI36
NG_046906.1:g.38413C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_013254.4:c.1207C>T MANE Select	NP_037386.1:p.His403Tyr
ENST00000331710.10:c.1207C>T MANE Select	ENSP00000329967.5:p.His403Tyr
NM_013254.3:c.1207C>T	NP_037386.1:p.His403Tyr
ENST00000331710.9:c.1207C>T	ENSP00000329967.5:p.His403Tyr
ENST00000536906.1:n.111C>T
ENST00000545025.1:n.477C>T
ENST00000545025.2:c.330C>T
ENST00000650708.1:c.1083C>T
ENST00000650762.1:c.1051C>T	ENSP00000498758.1:p.His351Tyr
ENST00000650786.1:c.*1352C>T	ENSP00000498280.1:n.*1352C>T
ENST00000650790.1:c.1207C>T	ENSP00000498995.1:p.His403Tyr
ENST00000650997.1:c.1207C>T	ENSP00000498341.1:p.His403Tyr
ENST00000651014.1:c.1051C>T	ENSP00000498885.1:p.His351Tyr
ENST00000651262.1:c.1207C>T	ENSP00000498461.1:p.His403Tyr
ENST00000651878.1:c.*691C>T	ENSP00000499077.1:n.*691C>T
ENST00000651889.1:n.958C>T
ENST00000651947.1:n.1295C>T
ENST00000652389.1:c.1207C>T	ENSP00000498414.1:p.His403Tyr
ENST00000652537.1:c.1207C>T	ENSP00000499102.1:p.His403Tyr
ENST00000652657.1:c.1207C>T	ENSP00000498887.1:p.His403Tyr
ENST00000676490.1:c.198-486C>T
ENST00000676539.1:c.18C>T
ENST00000676551.1:n.1306C>T
ENST00000676654.1:n.1336C>T
ENST00000676684.1:n.1336C>T
ENST00000676809.1:c.1207C>T	ENSP00000504298.1:p.His403Tyr
ENST00000676912.1:c.1051C>T	ENSP00000503567.1:p.His351Tyr
ENST00000676930.1:c.993-3015C>T	ENSP00000502899.1:n.993-3015C>T
ENST00000677499.1:c.1207C>T	ENSP00000502875.1:p.His403Tyr
ENST00000677632.1:c.1207C>T	ENSP00000504586.1:p.His403Tyr
ENST00000677641.1:c.1207C>T	ENSP00000504637.1:p.His403Tyr
ENST00000677686.1:n.3591C>T
ENST00000677831.1:c.1207C>T	ENSP00000503760.1:p.His403Tyr
ENST00000677858.1:c.271C>T
ENST00000678180.1:c.1207C>T	ENSP00000504132.1:p.His403Tyr
ENST00000678197.1:n.1190C>T
XM_005268809.1:c.1207C>T	XP_005268866.1:p.His403Tyr
XM_005268810.1:c.1207C>T	XP_005268867.1:p.His403Tyr
XR_001748674.2:n.1321C>T
XR_944524.1:n.1366C>T
XR_944525.1:n.1366C>T