Canonical Allele Identifier: CA2387297142
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886911G= , CM000683.2:g.34886911G= GRCh38
NC_000021.8:g.36259208G= , CM000683.1:g.36259208G= GRCh37
NC_000021.7:g.35181078G= NCBI36
NG_011402.2:g.1102801C= , LRG_482:g.1102801C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.283C= MANE Select ENSP00000501943.1:p.Pro95=
ENST00000300305.7:c.283C= ENSP00000300305.3:p.Pro95=
ENST00000344691.8:c.202C= ENSP00000340690.4:p.Pro68=
ENST00000358356.9:c.202C= ENSP00000351123.5:p.Pro68=
ENST00000399237.6:c.247C= ENSP00000382182.2:p.Pro83=
ENST00000399240.5:c.202C= ENSP00000382184.1:p.Pro68=
ENST00000437180.5:c.283C= ENSP00000409227.1:p.Pro95=
ENST00000455571.5:c.244C= ENSP00000388189.1:p.Pro82=
ENST00000482318.5:c.59-6198C= ENSP00000477067.1:n.59-6198C=
NM_001001890.2:c.202C= NP_001001890.1:p.Pro68=
NM_001122607.1:c.202C= NP_001116079.1:p.Pro68=
NM_001754.4:c.283C= , LRG_482t1:c.283C= NP_001745.2:p.Pro95=
XM_005261068.3:c.247C= XP_005261125.1:p.Pro83=
XM_005261069.3:c.283C= XP_005261126.1:p.Pro95=
XM_011529766.1:c.283C= XP_011528068.1:p.Pro95=
XM_011529767.1:c.244C= XP_011528069.1:p.Pro82=
XM_011529768.1:c.244C= XP_011528070.1:p.Pro82=
XM_011529770.1:c.283C= XP_011528072.1:p.Pro95=
XR_937576.1:n.462C=
XM_005261069.4:c.283C= XP_005261126.1:p.Pro95=
XM_011529766.2:c.283C= XP_011528068.1:p.Pro95=
XM_011529767.2:c.244C= XP_011528069.1:p.Pro82=
XM_011529768.2:c.244C= XP_011528070.1:p.Pro82=
XM_011529770.2:c.283C= XP_011528072.1:p.Pro95=
XM_017028487.1:c.130C= XP_016883976.1:p.Pro44=
XR_937576.2:n.509C=
NM_001001890.3:c.202C= NP_001001890.1:p.Pro68=
NM_001122607.2:c.202C= NP_001116079.1:p.Pro68=
NM_001754.5:c.283C= MANE Select NP_001745.2:p.Pro95=