Canonical Allele Identifier: CA645607439
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886902_34886903insT , CM000683.2:g.34886902_34886903insT GRCh38
NC_000021.8:g.36259199_36259200insT , CM000683.1:g.36259199_36259200insT GRCh37
NC_000021.7:g.35181069_35181070insT NCBI36
NG_011402.2:g.1102809_1102810insA , LRG_482:g.1102809_1102810insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.291_292insA MANE Select ENSP00000501943.1:p.Leu98ThrfsTer?
ENST00000300305.7:c.291_292insA ENSP00000300305.3:p.Leu98ThrfsTer?
ENST00000344691.8:c.210_211insA ENSP00000340690.4:p.Leu71ThrfsTer?
ENST00000358356.9:c.210_211insA ENSP00000351123.5:p.Leu71ThrfsTer?
ENST00000399237.6:c.255_256insA ENSP00000382182.2:p.Leu86ThrfsTer?
ENST00000399240.5:c.210_211insA ENSP00000382184.1:p.Leu71ThrfsTer?
ENST00000437180.5:c.291_292insA ENSP00000409227.1:p.Leu98ThrfsTer?
ENST00000455571.5:c.252_253insA ENSP00000388189.1:p.Leu85ThrfsTer?
ENST00000482318.5:c.59-6190_59-6189insA ENSP00000477067.1:n.59-6190_59-6189insA
NM_001001890.2:c.210_211insA NP_001001890.1:p.Leu71ThrfsTer?
NM_001122607.1:c.210_211insA NP_001116079.1:p.Leu71ThrfsTer?
NM_001754.4:c.291_292insA , LRG_482t1:c.291_292insA NP_001745.2:p.Leu98ThrfsTer?
XM_005261068.3:c.255_256insA XP_005261125.1:p.Leu86ThrfsTer?
XM_005261069.3:c.291_292insA XP_005261126.1:p.Leu98ThrfsTer?
XM_011529766.1:c.291_292insA XP_011528068.1:p.Leu98ThrfsTer?
XM_011529767.1:c.252_253insA XP_011528069.1:p.Leu85ThrfsTer?
XM_011529768.1:c.252_253insA XP_011528070.1:p.Leu85ThrfsTer?
XM_011529770.1:c.291_292insA XP_011528072.1:p.Leu98ThrfsTer?
XR_937576.1:n.470_471insA
XM_005261069.4:c.291_292insA XP_005261126.1:p.Leu98ThrfsTer?
XM_011529766.2:c.291_292insA XP_011528068.1:p.Leu98ThrfsTer?
XM_011529767.2:c.252_253insA XP_011528069.1:p.Leu85ThrfsTer?
XM_011529768.2:c.252_253insA XP_011528070.1:p.Leu85ThrfsTer?
XM_011529770.2:c.291_292insA XP_011528072.1:p.Leu98ThrfsTer?
XM_017028487.1:c.138_139insA XP_016883976.1:p.Leu47ThrfsTer?
XR_937576.2:n.517_518insA
NM_001001890.3:c.210_211insA NP_001001890.1:p.Leu71ThrfsTer?
NM_001122607.2:c.210_211insA NP_001116079.1:p.Leu71ThrfsTer?
NM_001754.5:c.291_292insA MANE Select NP_001745.2:p.Leu98ThrfsTer?