Canonical Allele Identifier: CA385592725

Gene: TBK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64455872T>C , CM000674.2:g.64455872T>C	GRCh38
NC_000012.11:g.64849652T>C , CM000674.1:g.64849652T>C	GRCh37
NC_000012.10:g.63135919T>C	NCBI36
NG_046906.1:g.8813T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_013254.4:c.2T>C MANE Select	NP_037386.1:p.Met1Thr
ENST00000331710.10:c.2T>C MANE Select	ENSP00000329967.5:p.Met1Thr
NM_013254.3:c.2T>C	NP_037386.1:p.Met1Thr
ENST00000331710.9:c.2T>C	ENSP00000329967.5:p.Met1Thr
ENST00000538890.5:c.2T>C	ENSP00000445834.1:p.Met1Thr
ENST00000539810.1:c.-110-45T>C	ENSP00000444428.1:n.-110-45T>C
ENST00000540417.1:c.2T>C	ENSP00000445628.1:p.Met1Thr
ENST00000650762.1:c.-110-45T>C	ENSP00000498758.1:n.-110-45T>C
ENST00000650786.1:c.2T>C	ENSP00000498280.1:p.Met1Thr
ENST00000650790.1:c.2T>C	ENSP00000498995.1:p.Met1Thr
ENST00000650997.1:c.2T>C	ENSP00000498341.1:p.Met1Thr
ENST00000651014.1:c.-266T>C	ENSP00000498885.1:n.-266T>C
ENST00000651262.1:c.2T>C	ENSP00000498461.1:p.Met1Thr
ENST00000651878.1:c.2T>C	ENSP00000499077.1:p.Met1Thr
ENST00000651947.1:n.90T>C
ENST00000652389.1:c.2T>C	ENSP00000498414.1:p.Met1Thr
ENST00000652537.1:c.2T>C	ENSP00000499102.1:p.Met1Thr
ENST00000652657.1:c.2T>C	ENSP00000498887.1:p.Met1Thr
ENST00000676469.1:c.2T>C	ENSP00000503155.1:p.Met1Thr
ENST00000676551.1:n.101T>C
ENST00000676654.1:n.131T>C
ENST00000676684.1:n.131T>C
ENST00000676809.1:c.2T>C	ENSP00000504298.1:p.Met1Thr
ENST00000676912.1:c.-97T>C	ENSP00000503567.1:n.-97T>C
ENST00000676930.1:c.2T>C	ENSP00000502899.1:p.Met1Thr
ENST00000677499.1:c.2T>C	ENSP00000502875.1:p.Met1Thr
ENST00000677545.1:c.-70+3685T>C	ENSP00000504729.1:n.-70+3685T>C
ENST00000677549.1:n.64T>C
ENST00000677632.1:c.2T>C	ENSP00000504586.1:p.Met1Thr
ENST00000677641.1:c.2T>C	ENSP00000504637.1:p.Met1Thr
ENST00000677686.1:n.105T>C
ENST00000677831.1:c.2T>C	ENSP00000503760.1:p.Met1Thr
ENST00000678180.1:c.2T>C	ENSP00000504132.1:p.Met1Thr
ENST00000678368.1:c.2T>C	ENSP00000504296.1:p.Met1Thr
ENST00000678430.1:n.101T>C
ENST00000679065.1:n.92T>C
XM_005268809.1:c.2T>C	XP_005268866.1:p.Met1Thr
XM_005268810.1:c.2T>C	XP_005268867.1:p.Met1Thr
XR_001748674.2:n.116T>C
XR_944524.1:n.161T>C
XR_944525.1:n.161T>C