Canonical Allele Identifier: CA2520067249

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15450543_15450544insGACACCCTCGTTTACAACGCCGATGCCTTCCAACTTTCGCATGGCTCGATGCTCGATGCGCTGATCGAGCAACTGCCGGGGGCGCAACTCAATGAGAGCGGCGTGATCACGGTGAACGGTAAGCGGGTG , CM000665.2:g.15450543_15450544insGACACCCTCGTTTACAACGCCGATGCCTTCCAACTTTCGCATGGCTCGATGCTCGATGCGCTGATCGAGCAACTGCCGGGGGCGCAACTCAATGAGAGCGGCGTGATCACGGTGAACGGTAAGCGGGTG GRCh38
NC_000003.11:g.15492050_15492051insGACACCCTCGTTTACAACGCCGATGCCTTCCAACTTTCGCATGGCTCGATGCTCGATGCGCTGATCGAGCAACTGCCGGGGGCGCAACTCAATGAGAGCGGCGTGATCACGGTGAACGGTAAGCGGGTG , CM000665.1:g.15492050_15492051insGACACCCTCGTTTACAACGCCGATGCCTTCCAACTTTCGCATGGCTCGATGCTCGATGCGCTGATCGAGCAACTGCCGGGGGCGCAACTCAATGAGAGCGGCGTGATCACGGTGAACGGTAAGCGGGTG GRCh37
NC_000003.10:g.15467054_15467055insGACACCCTCGTTTACAACGCCGATGCCTTCCAACTTTCGCATGGCTCGATGCTCGATGCGCTGATCGAGCAACTGCCGGGGGCGCAACTCAATGAGAGCGGCGTGATCACGGTGAACGGTAAGCGGGTG NCBI36
NG_009032.1:g.76208_76209insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC
NG_009032.2:g.76208_76209insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000608408.2:n.398+901_398+902insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (EAF1-AS1)
ENST00000626521.1:n.55+901_55+902insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (EAF1-AS1)
ENST00000629729.3:c.414+901_414+902insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC ENSP00000518887.1:n.414+901_414+902insCACCCGCTTACCGTTCACCGTGA...
ENST00000383788.10:c.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) MANE Select ENSP00000373298.3:n.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCAC...
ENST00000679838.1:c.*2230_*2231insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) ENSP00000505708.1:n.*2230_*2231insCACCCGCTTACCGTTCACCGTGATCAC...
ENST00000680545.1:n.2234_2235insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ)
ENST00000680897.1:n.1933_1934insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ)
ENST00000681097.1:c.*1482_*1483insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) ENSP00000505397.1:n.*1482_*1483insCACCCGCTTACCGTTCACCGTGATCAC...
ENST00000681222.1:n.5959_5960insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ)
ENST00000383781.8:c.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) ENSP00000373291.3:n.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCAC...
ENST00000383788.9:c.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) ENSP00000373298.3:n.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCAC...
ENST00000603752.1:n.336_337insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ)
ENST00000617675.1:n.464_465insGACACCCTCGTTTACAACGCCGATGCCTTCCAACTTTCGCATGGCTCGATGCTCGATGCGCTGATCGAGCAACTGCCGGGGGCGCAACTCAATGAGAGCGGCGTGATCACGGTGAACGGTAAGCGGGTG (EAF1)
NM_005677.3:c.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) NP_005668.2:n.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCT...
NM_080538.2:c.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) NP_536799.1:n.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCT...
NM_080539.3:c.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) NP_536800.2:n.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCT...
NM_005677.4:c.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) MANE Select NP_005668.2:n.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCT...
NM_080539.4:c.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCTCTCATTGAGTTGCGCCCCCGGCAGTTGCTCGATCAGCGCATCGAGCATCGAGCCATGCGAAAGTTGGAAGGCATCGGCGTTGTAAACGAGGGTGTC (COLQ) NP_536800.2:n.*1100_*1101insCACCCGCTTACCGTTCACCGTGATCACGCCGCT...