Canonical Allele Identifier: CA645607436
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886894_34886895insTTGCTCCTCTGCGAT , CM000683.2:g.34886894_34886895insTTGCTCCTCTGCGAT GRCh38
NC_000021.8:g.36259191_36259192insTTGCTCCTCTGCGAT , CM000683.1:g.36259191_36259192insTTGCTCCTCTGCGAT GRCh37
NC_000021.7:g.35181061_35181062insTTGCTCCTCTGCGAT NCBI36
NG_011402.2:g.1102817_1102818insATCGCAGAGGAGCAA , LRG_482:g.1102817_1102818insATCGCAGAGGAGCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.299_300insATCGCAGAGGAGCAA MANE Select ENSP00000501943.1:p.Ser100_Val101insSerGlnArgSerAsn
ENST00000300305.7:c.299_300insATCGCAGAGGAGCAA ENSP00000300305.3:p.Ser100_Val101insSerGlnArgSerAsn
ENST00000344691.8:c.218_219insATCGCAGAGGAGCAA ENSP00000340690.4:p.Ser73_Val74insSerGlnArgSerAsn
ENST00000358356.9:c.218_219insATCGCAGAGGAGCAA ENSP00000351123.5:p.Ser73_Val74insSerGlnArgSerAsn
ENST00000399237.6:c.263_264insATCGCAGAGGAGCAA ENSP00000382182.2:p.Ser88_Val89insSerGlnArgSerAsn
ENST00000399240.5:c.218_219insATCGCAGAGGAGCAA ENSP00000382184.1:p.Ser73_Val74insSerGlnArgSerAsn
ENST00000437180.5:c.299_300insATCGCAGAGGAGCAA ENSP00000409227.1:p.Ser100_Val101insSerGlnArgSerAsn
ENST00000455571.5:c.260_261insATCGCAGAGGAGCAA ENSP00000388189.1:p.Ser87_Val88insSerGlnArgSerAsn
ENST00000482318.5:c.59-6182_59-6181insATCGCAGAGGAGCAA ENSP00000477067.1:n.59-6182_59-6181insATCGCAGAGGAGCAA
NM_001001890.2:c.218_219insATCGCAGAGGAGCAA NP_001001890.1:p.Ser73_Val74insSerGlnArgSerAsn
NM_001122607.1:c.218_219insATCGCAGAGGAGCAA NP_001116079.1:p.Ser73_Val74insSerGlnArgSerAsn
NM_001754.4:c.299_300insATCGCAGAGGAGCAA , LRG_482t1:c.299_300insATCGCAGAGGAGCAA NP_001745.2:p.Ser100_Val101insSerGlnArgSerAsn
XM_005261068.3:c.263_264insATCGCAGAGGAGCAA XP_005261125.1:p.Ser88_Val89insSerGlnArgSerAsn
XM_005261069.3:c.299_300insATCGCAGAGGAGCAA XP_005261126.1:p.Ser100_Val101insSerGlnArgSerAsn
XM_011529766.1:c.299_300insATCGCAGAGGAGCAA XP_011528068.1:p.Ser100_Val101insSerGlnArgSerAsn
XM_011529767.1:c.260_261insATCGCAGAGGAGCAA XP_011528069.1:p.Ser87_Val88insSerGlnArgSerAsn
XM_011529768.1:c.260_261insATCGCAGAGGAGCAA XP_011528070.1:p.Ser87_Val88insSerGlnArgSerAsn
XM_011529770.1:c.299_300insATCGCAGAGGAGCAA XP_011528072.1:p.Ser100_Val101insSerGlnArgSerAsn
XR_937576.1:n.478_479insATCGCAGAGGAGCAA
XM_005261069.4:c.299_300insATCGCAGAGGAGCAA XP_005261126.1:p.Ser100_Val101insSerGlnArgSerAsn
XM_011529766.2:c.299_300insATCGCAGAGGAGCAA XP_011528068.1:p.Ser100_Val101insSerGlnArgSerAsn
XM_011529767.2:c.260_261insATCGCAGAGGAGCAA XP_011528069.1:p.Ser87_Val88insSerGlnArgSerAsn
XM_011529768.2:c.260_261insATCGCAGAGGAGCAA XP_011528070.1:p.Ser87_Val88insSerGlnArgSerAsn
XM_011529770.2:c.299_300insATCGCAGAGGAGCAA XP_011528072.1:p.Ser100_Val101insSerGlnArgSerAsn
XM_017028487.1:c.146_147insATCGCAGAGGAGCAA XP_016883976.1:p.Ser49_Val50insSerGlnArgSerAsn
XR_937576.2:n.525_526insATCGCAGAGGAGCAA
NM_001001890.3:c.218_219insATCGCAGAGGAGCAA NP_001001890.1:p.Ser73_Val74insSerGlnArgSerAsn
NM_001122607.2:c.218_219insATCGCAGAGGAGCAA NP_001116079.1:p.Ser73_Val74insSerGlnArgSerAsn
NM_001754.5:c.299_300insATCGCAGAGGAGCAA MANE Select NP_001745.2:p.Ser100_Val101insSerGlnArgSerAsn