Canonical Allele Identifier: CA2387297105
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs2057996989
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886837_34886838insG , CM000683.2:g.34886837_34886838insG GRCh38
NC_000021.8:g.36259134_36259135insG , CM000683.1:g.36259134_36259135insG GRCh37
NC_000021.7:g.35181004_35181005insG NCBI36
NG_011402.2:g.1102874_1102875insC , LRG_482:g.1102874_1102875insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.351+5_351+6insC MANE Select ENSP00000501943.1:n.351+5_351+6insC
ENST00000300305.7:c.351+5_351+6insC ENSP00000300305.3:n.351+5_351+6insC
ENST00000344691.8:c.270+5_270+6insC ENSP00000340690.4:n.270+5_270+6insC
ENST00000358356.9:c.270+5_270+6insC ENSP00000351123.5:n.270+5_270+6insC
ENST00000399237.6:c.315+5_315+6insC ENSP00000382182.2:n.315+5_315+6insC
ENST00000399240.5:c.270+5_270+6insC ENSP00000382184.1:n.270+5_270+6insC
ENST00000437180.5:c.351+5_351+6insC ENSP00000409227.1:n.351+5_351+6insC
ENST00000455571.5:c.312+5_312+6insC ENSP00000388189.1:n.312+5_312+6insC
ENST00000482318.5:c.59-6125_59-6124insC ENSP00000477067.1:n.59-6125_59-6124insC
NM_001001890.2:c.270+5_270+6insC NP_001001890.1:n.270+5_270+6insC
NM_001122607.1:c.270+5_270+6insC NP_001116079.1:n.270+5_270+6insC
NM_001754.4:c.351+5_351+6insC , LRG_482t1:c.351+5_351+6insC NP_001745.2:n.351+5_351+6insC
XM_005261068.3:c.315+5_315+6insC XP_005261125.1:n.315+5_315+6insC
XM_005261069.3:c.351+5_351+6insC XP_005261126.1:n.351+5_351+6insC
XM_011529766.1:c.351+5_351+6insC XP_011528068.1:n.351+5_351+6insC
XM_011529767.1:c.312+5_312+6insC XP_011528069.1:n.312+5_312+6insC
XM_011529768.1:c.312+5_312+6insC XP_011528070.1:n.312+5_312+6insC
XM_011529770.1:c.351+5_351+6insC XP_011528072.1:n.351+5_351+6insC
XR_937576.1:n.530+5_530+6insC
XM_005261069.4:c.351+5_351+6insC XP_005261126.1:n.351+5_351+6insC
XM_011529766.2:c.351+5_351+6insC XP_011528068.1:n.351+5_351+6insC
XM_011529767.2:c.312+5_312+6insC XP_011528069.1:n.312+5_312+6insC
XM_011529768.2:c.312+5_312+6insC XP_011528070.1:n.312+5_312+6insC
XM_011529770.2:c.351+5_351+6insC XP_011528072.1:n.351+5_351+6insC
XM_017028487.1:c.198+5_198+6insC XP_016883976.1:n.198+5_198+6insC
XR_937576.2:n.577+5_577+6insC
NM_001001890.3:c.270+5_270+6insC NP_001001890.1:n.270+5_270+6insC
NM_001122607.2:c.270+5_270+6insC NP_001116079.1:n.270+5_270+6insC
NM_001754.5:c.351+5_351+6insC MANE Select NP_001745.2:n.351+5_351+6insC
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