Canonical Allele Identifier: CA645607391
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM5879765 COSM5879766
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880642_34880643insAGG , CM000683.2:g.34880642_34880643insAGG GRCh38
NC_000021.8:g.36252939_36252940insAGG , CM000683.1:g.36252939_36252940insAGG GRCh37
NC_000021.7:g.35174809_35174810insAGG NCBI36
NG_011402.2:g.1109069_1109070insCCT , LRG_482:g.1109069_1109070insCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.422_423insCCT MANE Select ENSP00000501943.1:p.Ser141_Ala142insLeu
ENST00000300305.7:c.422_423insCCT ENSP00000300305.3:p.Ser141_Ala142insLeu
ENST00000344691.8:c.341_342insCCT ENSP00000340690.4:p.Ser114_Ala115insLeu
ENST00000358356.9:c.341_342insCCT ENSP00000351123.5:p.Ser114_Ala115insLeu
ENST00000399237.6:c.386_387insCCT ENSP00000382182.2:p.Ser129_Ala130insLeu
ENST00000399240.5:c.341_342insCCT ENSP00000382184.1:p.Ser114_Ala115insLeu
ENST00000437180.5:c.422_423insCCT ENSP00000409227.1:p.Ser141_Ala142insLeu
ENST00000455571.5:c.383_384insCCT ENSP00000388189.1:p.Ser128_Ala129insLeu
ENST00000482318.5:c.*12_*13insCCT ENSP00000477067.1:n.*12_*13insCCT
NM_001001890.2:c.341_342insCCT NP_001001890.1:p.Ser114_Ala115insLeu
NM_001122607.1:c.341_342insCCT NP_001116079.1:p.Ser114_Ala115insLeu
NM_001754.4:c.422_423insCCT , LRG_482t1:c.422_423insCCT NP_001745.2:p.Ser141_Ala142insLeu
XM_005261068.3:c.386_387insCCT XP_005261125.1:p.Ser129_Ala130insLeu
XM_005261069.3:c.422_423insCCT XP_005261126.1:p.Ser141_Ala142insLeu
XM_011529766.1:c.422_423insCCT XP_011528068.1:p.Ser141_Ala142insLeu
XM_011529767.1:c.383_384insCCT XP_011528069.1:p.Ser128_Ala129insLeu
XM_011529768.1:c.383_384insCCT XP_011528070.1:p.Ser128_Ala129insLeu
XM_011529770.1:c.422_423insCCT XP_011528072.1:p.Ser141_Ala142insLeu
XR_937576.1:n.601_602insCCT
XM_005261069.4:c.422_423insCCT XP_005261126.1:p.Ser141_Ala142insLeu
XM_011529766.2:c.422_423insCCT XP_011528068.1:p.Ser141_Ala142insLeu
XM_011529767.2:c.383_384insCCT XP_011528069.1:p.Ser128_Ala129insLeu
XM_011529768.2:c.383_384insCCT XP_011528070.1:p.Ser128_Ala129insLeu
XM_011529770.2:c.422_423insCCT XP_011528072.1:p.Ser141_Ala142insLeu
XM_017028487.1:c.269_270insCCT XP_016883976.1:p.Ser90_Ala91insLeu
XR_937576.2:n.648_649insCCT
NM_001001890.3:c.341_342insCCT NP_001001890.1:p.Ser114_Ala115insLeu
NM_001122607.2:c.341_342insCCT NP_001116079.1:p.Ser114_Ala115insLeu
NM_001754.5:c.422_423insCCT MANE Select NP_001745.2:p.Ser141_Ala142insLeu
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