Canonical Allele Identifier: CA6669024
Community Standard Title: NM_013254.4(TBK1):c.1260G>C (p.Gly420=)
Gene: TBK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.64485937G>C , CM000674.2:g.64485937G>C GRCh38
NC_000012.11:g.64879717G>C , CM000674.1:g.64879717G>C GRCh37
NC_000012.10:g.63165984G>C NCBI36
NG_046906.1:g.38878G>C

Transcript Alleles

HGVS Amino-acid Change
NM_013254.4:c.1260G>C MANE Select NP_037386.1:p.Gly420=
ENST00000331710.10:c.1260G>C MANE Select ENSP00000329967.5:p.Gly420=
NM_013254.3:c.1260G>C NP_037386.1:p.Gly420=
ENST00000331710.9:c.1260G>C ENSP00000329967.5:p.Gly420=
ENST00000536906.1:n.576G>C
ENST00000650708.1:c.1136G>C
ENST00000650762.1:c.1104G>C ENSP00000498758.1:p.Gly368=
ENST00000650786.1:c.*1405G>C ENSP00000498280.1:n.*1405G>C
ENST00000650790.1:c.1260G>C ENSP00000498995.1:p.Gly420=
ENST00000650997.1:c.1260G>C ENSP00000498341.1:p.Gly420=
ENST00000651014.1:c.1104G>C ENSP00000498885.1:p.Gly368=
ENST00000651262.1:c.1260G>C ENSP00000498461.1:p.Gly420=
ENST00000651878.1:c.*744G>C ENSP00000499077.1:n.*744G>C
ENST00000651889.1:n.1000-21G>C
ENST00000651947.1:n.1348G>C
ENST00000652389.1:c.1260G>C ENSP00000498414.1:p.Gly420=
ENST00000652537.1:c.1260G>C ENSP00000499102.1:p.Gly420=
ENST00000652657.1:c.1260G>C ENSP00000498887.1:p.Gly420=
ENST00000676490.1:c.198-21G>C
ENST00000676539.1:c.60-21G>C
ENST00000676551.1:n.1359G>C
ENST00000676654.1:n.1389G>C
ENST00000676684.1:n.1389G>C
ENST00000676774.1:n.115G>C
ENST00000676809.1:c.1260G>C ENSP00000504298.1:p.Gly420=
ENST00000676912.1:c.1104G>C ENSP00000503567.1:p.Gly368=
ENST00000676930.1:c.993-2550G>C ENSP00000502899.1:n.993-2550G>C
ENST00000677499.1:c.1260G>C ENSP00000502875.1:p.Gly420=
ENST00000677632.1:c.1260G>C ENSP00000504586.1:p.Gly420=
ENST00000677641.1:c.1260G>C ENSP00000504637.1:p.Gly420=
ENST00000677686.1:n.3644G>C
ENST00000677831.1:c.1260G>C ENSP00000503760.1:p.Gly420=
ENST00000678180.1:c.1260G>C ENSP00000504132.1:p.Gly420=
ENST00000678197.1:n.1243G>C
ENST00000678582.1:c.12G>C ENSP00000504002.1:p.Gly4=
XM_005268809.1:c.1260G>C XP_005268866.1:p.Gly420=
XM_005268810.1:c.1260G>C XP_005268867.1:p.Gly420=
XR_001748674.2:n.1374G>C
XR_944524.1:n.1419G>C
XR_944525.1:n.1419G>C