Canonical Allele Identifier: CA385592734

Gene: TBK1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.64455874C>T , CM000674.2:g.64455874C>T	GRCh38
NC_000012.11:g.64849654C>T , CM000674.1:g.64849654C>T	GRCh37
NC_000012.10:g.63135921C>T	NCBI36
NG_046906.1:g.8815C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_013254.4:c.4C>T MANE Select	NP_037386.1:p.Gln2Ter
ENST00000331710.10:c.4C>T MANE Select	ENSP00000329967.5:p.Gln2Ter
NM_013254.3:c.4C>T	NP_037386.1:p.Gln2Ter
ENST00000331710.9:c.4C>T	ENSP00000329967.5:p.Gln2Ter
ENST00000538890.5:c.4C>T	ENSP00000445834.1:p.Gln2Ter
ENST00000539810.1:c.-110-43C>T	ENSP00000444428.1:n.-110-43C>T
ENST00000540417.1:c.4C>T	ENSP00000445628.1:p.Gln2Ter
ENST00000650762.1:c.-110-43C>T	ENSP00000498758.1:n.-110-43C>T
ENST00000650786.1:c.4C>T	ENSP00000498280.1:p.Gln2Ter
ENST00000650790.1:c.4C>T	ENSP00000498995.1:p.Gln2Ter
ENST00000650997.1:c.4C>T	ENSP00000498341.1:p.Gln2Ter
ENST00000651014.1:c.-264C>T	ENSP00000498885.1:n.-264C>T
ENST00000651262.1:c.4C>T	ENSP00000498461.1:p.Gln2Ter
ENST00000651878.1:c.4C>T	ENSP00000499077.1:p.Gln2Ter
ENST00000651947.1:n.92C>T
ENST00000652389.1:c.4C>T	ENSP00000498414.1:p.Gln2Ter
ENST00000652537.1:c.4C>T	ENSP00000499102.1:p.Gln2Ter
ENST00000652657.1:c.4C>T	ENSP00000498887.1:p.Gln2Ter
ENST00000676469.1:c.4C>T	ENSP00000503155.1:p.Gln2Ter
ENST00000676551.1:n.103C>T
ENST00000676654.1:n.133C>T
ENST00000676684.1:n.133C>T
ENST00000676809.1:c.4C>T	ENSP00000504298.1:p.Gln2Ter
ENST00000676912.1:c.-95C>T	ENSP00000503567.1:n.-95C>T
ENST00000676930.1:c.4C>T	ENSP00000502899.1:p.Gln2Ter
ENST00000677499.1:c.4C>T	ENSP00000502875.1:p.Gln2Ter
ENST00000677545.1:c.-70+3687C>T	ENSP00000504729.1:n.-70+3687C>T
ENST00000677549.1:n.66C>T
ENST00000677632.1:c.4C>T	ENSP00000504586.1:p.Gln2Ter
ENST00000677641.1:c.4C>T	ENSP00000504637.1:p.Gln2Ter
ENST00000677686.1:n.107C>T
ENST00000677831.1:c.4C>T	ENSP00000503760.1:p.Gln2Ter
ENST00000678180.1:c.4C>T	ENSP00000504132.1:p.Gln2Ter
ENST00000678368.1:c.4C>T	ENSP00000504296.1:p.Gln2Ter
ENST00000678430.1:n.103C>T
ENST00000679065.1:n.94C>T
XM_005268809.1:c.4C>T	XP_005268866.1:p.Gln2Ter
XM_005268810.1:c.4C>T	XP_005268867.1:p.Gln2Ter
XR_001748674.2:n.118C>T
XR_944524.1:n.163C>T
XR_944525.1:n.163C>T