Canonical Allele Identifier: CA385595952

Gene: TBK1

Linked Data

• MyVariant Identifiers: chr12:g.64860725G>T (hg19) ; chr12:g.64466945G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64466945G>T , CM000674.2:g.64466945G>T	GRCh38
NC_000012.11:g.64860725G>T , CM000674.1:g.64860725G>T	GRCh37
NC_000012.10:g.63146992G>T	NCBI36
NG_046906.1:g.19886G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331710.10:c.403G>T MANE Select	ENSP00000329967.5:p.Asp135Tyr
ENST00000650708.1:c.279G>T
ENST00000650762.1:c.247G>T	ENSP00000498758.1:p.Asp83Tyr
ENST00000650786.1:c.*548G>T	ENSP00000498280.1:n.*548G>T
ENST00000650790.1:c.403G>T	ENSP00000498995.1:p.Asp135Tyr
ENST00000650997.1:c.403G>T	ENSP00000498341.1:p.Asp135Tyr
ENST00000651014.1:c.247G>T	ENSP00000498885.1:p.Asp83Tyr
ENST00000651262.1:c.403G>T	ENSP00000498461.1:p.Asp135Tyr
ENST00000651878.1:c.403G>T	ENSP00000499077.1:p.Asp135Tyr
ENST00000651889.1:n.154G>T
ENST00000651947.1:n.491G>T
ENST00000652389.1:c.403G>T	ENSP00000498414.1:p.Asp135Tyr
ENST00000652537.1:c.403G>T	ENSP00000499102.1:p.Asp135Tyr
ENST00000652657.1:c.403G>T	ENSP00000498887.1:p.Asp135Tyr
ENST00000676551.1:n.502G>T
ENST00000676654.1:n.532G>T
ENST00000676684.1:n.532G>T
ENST00000676809.1:c.403G>T	ENSP00000504298.1:p.Asp135Tyr
ENST00000676912.1:c.247G>T	ENSP00000503567.1:p.Asp83Tyr
ENST00000676930.1:c.403G>T	ENSP00000502899.1:p.Asp135Tyr
ENST00000677016.1:c.45G>T
ENST00000677112.1:c.45G>T
ENST00000677499.1:c.403G>T	ENSP00000502875.1:p.Asp135Tyr
ENST00000677549.1:n.465G>T
ENST00000677632.1:c.403G>T	ENSP00000504586.1:p.Asp135Tyr
ENST00000677641.1:c.403G>T	ENSP00000504637.1:p.Asp135Tyr
ENST00000677686.1:n.506G>T
ENST00000677759.1:c.260G>T	ENSP00000503847.1:p.Ter87Leu
ENST00000677831.1:c.403G>T	ENSP00000503760.1:p.Asp135Tyr
ENST00000677973.1:c.45G>T
ENST00000678079.1:c.131-34G>T	ENSP00000503613.1:n.131-34G>T
ENST00000678180.1:c.403G>T	ENSP00000504132.1:p.Asp135Tyr
ENST00000678197.1:n.387G>T
ENST00000678738.1:c.45G>T
ENST00000678808.1:c.45G>T
ENST00000679050.1:c.365G>T	ENSP00000503595.1:n.365G>T
ENST00000679302.1:c.171G>T	ENSP00000503553.1:n.171G>T
ENST00000331710.9:c.403G>T	ENSP00000329967.5:p.Asp135Tyr
NM_013254.3:c.403G>T	NP_037386.1:p.Asp135Tyr
XM_005268809.1:c.403G>T	XP_005268866.1:p.Asp135Tyr
XM_005268810.1:c.403G>T	XP_005268867.1:p.Asp135Tyr
XR_944524.1:n.562G>T
XR_944525.1:n.562G>T
XR_001748674.2:n.517G>T
NM_013254.4:c.403G>T MANE Select	NP_037386.1:p.Asp135Tyr