Canonical Allele Identifier: CA645607356
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM24717
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880621_34880626dup , CM000683.2:g.34880621_34880626dup GRCh38
NC_000021.8:g.36252918_36252923dup , CM000683.1:g.36252918_36252923dup GRCh37
NC_000021.7:g.35174788_35174793dup NCBI36
NG_011402.2:g.1109088_1109093dup , LRG_482:g.1109088_1109093dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.441_446dup MANE Select ENSP00000501943.1:p.Ala149_Ala150insThrAla
ENST00000300305.7:c.441_446dup ENSP00000300305.3:p.Ala149_Ala150insThrAla
ENST00000344691.8:c.360_365dup ENSP00000340690.4:p.Ala122_Ala123insThrAla
ENST00000358356.9:c.360_365dup ENSP00000351123.5:p.Ala122_Ala123insThrAla
ENST00000399237.6:c.405_410dup ENSP00000382182.2:p.Ala137_Ala138insThrAla
ENST00000399240.5:c.360_365dup ENSP00000382184.1:p.Ala122_Ala123insThrAla
ENST00000437180.5:c.441_446dup ENSP00000409227.1:p.Ala149_Ala150insThrAla
ENST00000455571.5:c.402_407dup ENSP00000388189.1:p.Ala136_Ala137insThrAla
ENST00000482318.5:c.*31_*36dup ENSP00000477067.1:n.*31_*36dup
NM_001001890.2:c.360_365dup NP_001001890.1:p.Ala122_Ala123insThrAla
NM_001122607.1:c.360_365dup NP_001116079.1:p.Ala122_Ala123insThrAla
NM_001754.4:c.441_446dup , LRG_482t1:c.441_446dup NP_001745.2:p.Ala149_Ala150insThrAla
XM_005261068.3:c.405_410dup XP_005261125.1:p.Ala137_Ala138insThrAla
XM_005261069.3:c.441_446dup XP_005261126.1:p.Ala149_Ala150insThrAla
XM_011529766.1:c.441_446dup XP_011528068.1:p.Ala149_Ala150insThrAla
XM_011529767.1:c.402_407dup XP_011528069.1:p.Ala136_Ala137insThrAla
XM_011529768.1:c.402_407dup XP_011528070.1:p.Ala136_Ala137insThrAla
XM_011529770.1:c.441_446dup XP_011528072.1:p.Ala149_Ala150insThrAla
XR_937576.1:n.620_625dup
XM_005261069.4:c.441_446dup XP_005261126.1:p.Ala149_Ala150insThrAla
XM_011529766.2:c.441_446dup XP_011528068.1:p.Ala149_Ala150insThrAla
XM_011529767.2:c.402_407dup XP_011528069.1:p.Ala136_Ala137insThrAla
XM_011529768.2:c.402_407dup XP_011528070.1:p.Ala136_Ala137insThrAla
XM_011529770.2:c.441_446dup XP_011528072.1:p.Ala149_Ala150insThrAla
XM_017028487.1:c.288_293dup XP_016883976.1:p.Ala98_Ala99insThrAla
XR_937576.2:n.667_672dup
NM_001001890.3:c.360_365dup NP_001001890.1:p.Ala122_Ala123insThrAla
NM_001122607.2:c.360_365dup NP_001116079.1:p.Ala122_Ala123insThrAla
NM_001754.5:c.441_446dup MANE Select NP_001745.2:p.Ala149_Ala150insThrAla
Search 100 bp 5'
Search 100 bp 3'