Canonical Allele Identifier: CA2387272266
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34834470G= , CM000683.2:g.34834470G= GRCh38
NC_000021.8:g.36206767G= , CM000683.1:g.36206767G= GRCh37
NC_000021.7:g.35128637G= NCBI36
NG_011402.2:g.1155242C= , LRG_482:g.1155242C=

Transcript Alleles

HGVS Amino-acid change
ENST00000675419.1:c.745C= MANE Select ENSP00000501943.1:p.Pro249=
ENST00000300305.7:c.745C= ENSP00000300305.3:p.Pro249=
ENST00000344691.8:c.664C= ENSP00000340690.4:p.Pro222=
ENST00000358356.9:c.664C= ENSP00000351123.5:p.Pro222=
ENST00000399237.6:c.709C= ENSP00000382182.2:p.Pro237=
ENST00000399240.5:c.532+25004C= ENSP00000382184.1:n.532+25004C=
ENST00000437180.5:c.745C= ENSP00000409227.1:p.Pro249=
ENST00000469087.1:n.281C=
ENST00000482318.5:c.*335C= ENSP00000477067.1:n.*335C=
NM_001001890.2:c.664C= NP_001001890.1:p.Pro222=
NM_001122607.1:c.664C= NP_001116079.1:p.Pro222=
NM_001754.4:c.745C= , LRG_482t1:c.745C= NP_001745.2:p.Pro249=
XM_005261068.3:c.709C= XP_005261125.1:p.Pro237=
XM_005261069.3:c.613+25004C= XP_005261126.1:n.613+25004C=
XM_011529766.1:c.745C= XP_011528068.1:p.Pro249=
XM_011529767.1:c.706C= XP_011528069.1:p.Pro236=
XM_011529768.1:c.574+25004C= XP_011528070.1:n.574+25004C=
XM_011529770.1:c.745C= XP_011528072.1:p.Pro249=
XR_937576.1:n.924C=
XM_005261069.4:c.613+25004C= XP_005261126.1:n.613+25004C=
XM_011529766.2:c.745C= XP_011528068.1:p.Pro249=
XM_011529767.2:c.706C= XP_011528069.1:p.Pro236=
XM_011529768.2:c.574+25004C= XP_011528070.1:n.574+25004C=
XM_011529770.2:c.745C= XP_011528072.1:p.Pro249=
XM_017028487.1:c.592C= XP_016883976.1:p.Pro198=
XR_937576.2:n.971C=
NM_001001890.3:c.664C= NP_001001890.1:p.Pro222=
NM_001122607.2:c.664C= NP_001116079.1:p.Pro222=
NM_001754.5:c.745C= MANE Select NP_001745.2:p.Pro249=