Canonical Allele Identifier: CA645607437
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM25126

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886897_34886898insTCTG , CM000683.2:g.34886897_34886898insTCTG GRCh38
NC_000021.8:g.36259194_36259195insTCTG , CM000683.1:g.36259194_36259195insTCTG GRCh37
NC_000021.7:g.35181064_35181065insTCTG NCBI36
NG_011402.2:g.1102815_1102816insAGAC , LRG_482:g.1102815_1102816insAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.297_298insAGAC MANE Select ENSP00000501943.1:p.Ser100ArgfsTer?
ENST00000300305.7:c.297_298insAGAC ENSP00000300305.3:p.Ser100ArgfsTer?
ENST00000344691.8:c.216_217insAGAC ENSP00000340690.4:p.Ser73ArgfsTer?
ENST00000358356.9:c.216_217insAGAC ENSP00000351123.5:p.Ser73ArgfsTer?
ENST00000399237.6:c.261_262insAGAC ENSP00000382182.2:p.Ser88ArgfsTer?
ENST00000399240.5:c.216_217insAGAC ENSP00000382184.1:p.Ser73ArgfsTer?
ENST00000437180.5:c.297_298insAGAC ENSP00000409227.1:p.Ser100ArgfsTer?
ENST00000455571.5:c.258_259insAGAC ENSP00000388189.1:p.Ser87ArgfsTer?
ENST00000482318.5:c.59-6184_59-6183insAGAC ENSP00000477067.1:n.59-6184_59-6183insAGAC
NM_001001890.2:c.216_217insAGAC NP_001001890.1:p.Ser73ArgfsTer?
NM_001122607.1:c.216_217insAGAC NP_001116079.1:p.Ser73ArgfsTer?
NM_001754.4:c.297_298insAGAC , LRG_482t1:c.297_298insAGAC NP_001745.2:p.Ser100ArgfsTer?
XM_005261068.3:c.261_262insAGAC XP_005261125.1:p.Ser88ArgfsTer?
XM_005261069.3:c.297_298insAGAC XP_005261126.1:p.Ser100ArgfsTer?
XM_011529766.1:c.297_298insAGAC XP_011528068.1:p.Ser100ArgfsTer?
XM_011529767.1:c.258_259insAGAC XP_011528069.1:p.Ser87ArgfsTer?
XM_011529768.1:c.258_259insAGAC XP_011528070.1:p.Ser87ArgfsTer?
XM_011529770.1:c.297_298insAGAC XP_011528072.1:p.Ser100ArgfsTer?
XR_937576.1:n.476_477insAGAC
XM_005261069.4:c.297_298insAGAC XP_005261126.1:p.Ser100ArgfsTer?
XM_011529766.2:c.297_298insAGAC XP_011528068.1:p.Ser100ArgfsTer?
XM_011529767.2:c.258_259insAGAC XP_011528069.1:p.Ser87ArgfsTer?
XM_011529768.2:c.258_259insAGAC XP_011528070.1:p.Ser87ArgfsTer?
XM_011529770.2:c.297_298insAGAC XP_011528072.1:p.Ser100ArgfsTer?
XM_017028487.1:c.144_145insAGAC XP_016883976.1:p.Ser49ArgfsTer?
XR_937576.2:n.523_524insAGAC
NM_001001890.3:c.216_217insAGAC NP_001001890.1:p.Ser73ArgfsTer?
NM_001122607.2:c.216_217insAGAC NP_001116079.1:p.Ser73ArgfsTer?
NM_001754.5:c.297_298insAGAC MANE Select NP_001745.2:p.Ser100ArgfsTer?