Canonical Allele Identifier: CA2042165381
Gene: TBK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.64466853A= , CM000674.2:g.64466853A= GRCh38
NC_000012.11:g.64860633A= , CM000674.1:g.64860633A= GRCh37
NC_000012.10:g.63146900A= NCBI36
NG_046906.1:g.19794A=

Transcript Alleles

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