Canonical Allele Identifier: CA512318810
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886842_34886843insG , CM000683.2:g.34886842_34886843insG GRCh38
NC_000021.8:g.36259139_36259140insG , CM000683.1:g.36259139_36259140insG GRCh37
NC_000021.7:g.35181009_35181010insG NCBI36
NG_011402.2:g.1102869_1102870insC , LRG_482:g.1102869_1102870insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.351_351+1insC MANE Select ENSP00000501943.1:n.351_351+1insC
ENST00000300305.7:c.351_351+1insC ENSP00000300305.3:n.351_351+1insC
ENST00000344691.8:c.270_270+1insC ENSP00000340690.4:n.270_270+1insC
ENST00000358356.9:c.270_270+1insC ENSP00000351123.5:n.270_270+1insC
ENST00000399237.6:c.315_315+1insC ENSP00000382182.2:n.315_315+1insC
ENST00000399240.5:c.270_270+1insC ENSP00000382184.1:n.270_270+1insC
ENST00000437180.5:c.351_351+1insC ENSP00000409227.1:n.351_351+1insC
ENST00000455571.5:c.312_312+1insC ENSP00000388189.1:n.312_312+1insC
ENST00000482318.5:c.59-6130_59-6129insC ENSP00000477067.1:n.59-6130_59-6129insC
NM_001001890.2:c.270_270+1insC NP_001001890.1:n.270_270+1insC
NM_001122607.1:c.270_270+1insC NP_001116079.1:n.270_270+1insC
NM_001754.4:c.351_351+1insC , LRG_482t1:c.351_351+1insC NP_001745.2:n.351_351+1insC
XM_005261068.3:c.315_315+1insC XP_005261125.1:n.315_315+1insC
XM_005261069.3:c.351_351+1insC XP_005261126.1:n.351_351+1insC
XM_011529766.1:c.351_351+1insC XP_011528068.1:n.351_351+1insC
XM_011529767.1:c.312_312+1insC XP_011528069.1:n.312_312+1insC
XM_011529768.1:c.312_312+1insC XP_011528070.1:n.312_312+1insC
XM_011529770.1:c.351_351+1insC XP_011528072.1:n.351_351+1insC
XR_937576.1:n.530_530+1insC
XM_005261069.4:c.351_351+1insC XP_005261126.1:n.351_351+1insC
XM_011529766.2:c.351_351+1insC XP_011528068.1:n.351_351+1insC
XM_011529767.2:c.312_312+1insC XP_011528069.1:n.312_312+1insC
XM_011529768.2:c.312_312+1insC XP_011528070.1:n.312_312+1insC
XM_011529770.2:c.351_351+1insC XP_011528072.1:n.351_351+1insC
XM_017028487.1:c.198_198+1insC XP_016883976.1:n.198_198+1insC
XR_937576.2:n.577_577+1insC
NM_001001890.3:c.270_270+1insC NP_001001890.1:n.270_270+1insC
NM_001122607.2:c.270_270+1insC NP_001116079.1:n.270_270+1insC
NM_001754.5:c.351_351+1insC MANE Select NP_001745.2:n.351_351+1insC