Canonical Allele Identifier: CA645607368
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM1180466
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880633_34880641delinsGGGGGT , CM000683.2:g.34880633_34880641delinsGGGGGT GRCh38
NC_000021.8:g.36252930_36252938delinsGGGGGT , CM000683.1:g.36252930_36252938delinsGGGGGT GRCh37
NC_000021.7:g.35174800_35174808delinsGGGGGT NCBI36
NG_011402.2:g.1109071_1109079delinsACCCCC , LRG_482:g.1109071_1109079delinsACCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.424_432delinsACCCCC MANE Select ENSP00000501943.1:p.Ala142_Leu144delinsThrPro
ENST00000300305.7:c.424_432delinsACCCCC ENSP00000300305.3:p.Ala142_Leu144delinsThrPro
ENST00000344691.8:c.343_351delinsACCCCC ENSP00000340690.4:p.Ala115_Leu117delinsThrPro
ENST00000358356.9:c.343_351delinsACCCCC ENSP00000351123.5:p.Ala115_Leu117delinsThrPro
ENST00000399237.6:c.388_396delinsACCCCC ENSP00000382182.2:p.Ala130_Leu132delinsThrPro
ENST00000399240.5:c.343_351delinsACCCCC ENSP00000382184.1:p.Ala115_Leu117delinsThrPro
ENST00000437180.5:c.424_432delinsACCCCC ENSP00000409227.1:p.Ala142_Leu144delinsThrPro
ENST00000455571.5:c.385_393delinsACCCCC ENSP00000388189.1:p.Ala129_Leu131delinsThrPro
ENST00000482318.5:c.*14_*22delinsACCCCC ENSP00000477067.1:n.*14_*22delinsACCCCC
NM_001001890.2:c.343_351delinsACCCCC NP_001001890.1:p.Ala115_Leu117delinsThrPro
NM_001122607.1:c.343_351delinsACCCCC NP_001116079.1:p.Ala115_Leu117delinsThrPro
NM_001754.4:c.424_432delinsACCCCC , LRG_482t1:c.424_432delinsACCCCC NP_001745.2:p.Ala142_Leu144delinsThrPro
XM_005261068.3:c.388_396delinsACCCCC XP_005261125.1:p.Ala130_Leu132delinsThrPro
XM_005261069.3:c.424_432delinsACCCCC XP_005261126.1:p.Ala142_Leu144delinsThrPro
XM_011529766.1:c.424_432delinsACCCCC XP_011528068.1:p.Ala142_Leu144delinsThrPro
XM_011529767.1:c.385_393delinsACCCCC XP_011528069.1:p.Ala129_Leu131delinsThrPro
XM_011529768.1:c.385_393delinsACCCCC XP_011528070.1:p.Ala129_Leu131delinsThrPro
XM_011529770.1:c.424_432delinsACCCCC XP_011528072.1:p.Ala142_Leu144delinsThrPro
XR_937576.1:n.603_611delinsACCCCC
XM_005261069.4:c.424_432delinsACCCCC XP_005261126.1:p.Ala142_Leu144delinsThrPro
XM_011529766.2:c.424_432delinsACCCCC XP_011528068.1:p.Ala142_Leu144delinsThrPro
XM_011529767.2:c.385_393delinsACCCCC XP_011528069.1:p.Ala129_Leu131delinsThrPro
XM_011529768.2:c.385_393delinsACCCCC XP_011528070.1:p.Ala129_Leu131delinsThrPro
XM_011529770.2:c.424_432delinsACCCCC XP_011528072.1:p.Ala142_Leu144delinsThrPro
XM_017028487.1:c.271_279delinsACCCCC XP_016883976.1:p.Ala91_Leu93delinsThrPro
XR_937576.2:n.650_658delinsACCCCC
NM_001001890.3:c.343_351delinsACCCCC NP_001001890.1:p.Ala115_Leu117delinsThrPro
NM_001122607.2:c.343_351delinsACCCCC NP_001116079.1:p.Ala115_Leu117delinsThrPro
NM_001754.5:c.424_432delinsACCCCC MANE Select NP_001745.2:p.Ala142_Leu144delinsThrPro
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