Canonical Allele Identifier: CA645607420

Gene: RUNX1

Linked Data

• COSMIC: COSM1717870

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886851_34886855del , CM000683.2:g.34886851_34886855del	GRCh38
NC_000021.8:g.36259148_36259152del , CM000683.1:g.36259148_36259152del	GRCh37
NC_000021.7:g.35181018_35181022del	NCBI36
NG_011402.2:g.1102858_1102862del , LRG_482:g.1102858_1102862del

Transcript Alleles

HGVS	Amino-acid change
ENST00000675419.1:c.340_344del MANE Select	ENSP00000501943.1:p.Ile114PhefsTer22
ENST00000300305.7:c.340_344del	ENSP00000300305.3:p.Ile114PhefsTer22
ENST00000344691.8:c.259_263del	ENSP00000340690.4:p.Ile87PhefsTer22
ENST00000358356.9:c.259_263del	ENSP00000351123.5:p.Ile87PhefsTer22
ENST00000399237.6:c.304_308del	ENSP00000382182.2:p.Ile102PhefsTer22
ENST00000399240.5:c.259_263del	ENSP00000382184.1:p.Ile87PhefsTer22
ENST00000437180.5:c.340_344del	ENSP00000409227.1:p.Ile114PhefsTer22
ENST00000455571.5:c.301_305del	ENSP00000388189.1:p.Ile101PhefsTer22
ENST00000482318.5:c.59-6141_59-6137del	ENSP00000477067.1:n.59-6141_59-6137del
NM_001001890.2:c.259_263del	NP_001001890.1:p.Ile87PhefsTer22
NM_001122607.1:c.259_263del	NP_001116079.1:p.Ile87PhefsTer22
NM_001754.4:c.340_344del , LRG_482t1:c.340_344del	NP_001745.2:p.Ile114PhefsTer22
XM_005261068.3:c.304_308del	XP_005261125.1:p.Ile102PhefsTer22
XM_005261069.3:c.340_344del	XP_005261126.1:p.Ile114PhefsTer22
XM_011529766.1:c.340_344del	XP_011528068.1:p.Ile114PhefsTer22
XM_011529767.1:c.301_305del	XP_011528069.1:p.Ile101PhefsTer22
XM_011529768.1:c.301_305del	XP_011528070.1:p.Ile101PhefsTer22
XM_011529770.1:c.340_344del	XP_011528072.1:p.Ile114PhefsTer22
XR_937576.1:n.519_523del
XM_005261069.4:c.340_344del	XP_005261126.1:p.Ile114PhefsTer22
XM_011529766.2:c.340_344del	XP_011528068.1:p.Ile114PhefsTer22
XM_011529767.2:c.301_305del	XP_011528069.1:p.Ile101PhefsTer22
XM_011529768.2:c.301_305del	XP_011528070.1:p.Ile101PhefsTer22
XM_011529770.2:c.340_344del	XP_011528072.1:p.Ile114PhefsTer22
XM_017028487.1:c.187_191del	XP_016883976.1:p.Ile63PhefsTer22
XR_937576.2:n.566_570del
NM_001001890.3:c.259_263del	NP_001001890.1:p.Ile87PhefsTer22
NM_001122607.2:c.259_263del	NP_001116079.1:p.Ile87PhefsTer22
NM_001754.5:c.340_344del MANE Select	NP_001745.2:p.Ile114PhefsTer22