Canonical Allele Identifier: CA2387297270
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887133A= , CM000683.2:g.34887133A= GRCh38
NC_000021.8:g.36259430A= , CM000683.1:g.36259430A= GRCh37
NC_000021.7:g.35181300A= NCBI36
NG_011402.2:g.1102579T= , LRG_482:g.1102579T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.98-37T= MANE Select ENSP00000501943.1:n.98-37T=
ENST00000300305.7:c.98-37T= ENSP00000300305.3:n.98-37T=
ENST00000344691.8:c.-21T= ENSP00000340690.4:n.-21T=
ENST00000358356.9:c.-21T= ENSP00000351123.5:n.-21T=
ENST00000399237.6:c.62-37T= ENSP00000382182.2:n.62-37T=
ENST00000399240.5:c.-21T= ENSP00000382184.1:n.-21T=
ENST00000437180.5:c.98-37T= ENSP00000409227.1:n.98-37T=
ENST00000455571.5:c.59-37T= ENSP00000388189.1:n.59-37T=
ENST00000475045.6:c.98-37T= ENSP00000477072.1:n.98-37T=
ENST00000482318.5:c.59-6420T= ENSP00000477067.1:n.59-6420T=
NM_001001890.2:c.-21T= NP_001001890.1:n.-21T=
NM_001122607.1:c.-21T= NP_001116079.1:n.-21T=
NM_001754.4:c.98-37T= , LRG_482t1:c.98-37T= NP_001745.2:n.98-37T=
XM_005261068.3:c.62-37T= XP_005261125.1:n.62-37T=
XM_005261069.3:c.98-37T= XP_005261126.1:n.98-37T=
XM_011529766.1:c.98-37T= XP_011528068.1:n.98-37T=
XM_011529767.1:c.59-37T= XP_011528069.1:n.59-37T=
XM_011529768.1:c.59-37T= XP_011528070.1:n.59-37T=
XM_011529770.1:c.98-37T= XP_011528072.1:n.98-37T=
XR_937576.1:n.277-37T=
XM_005261069.4:c.98-37T= XP_005261126.1:n.98-37T=
XM_011529766.2:c.98-37T= XP_011528068.1:n.98-37T=
XM_011529767.2:c.59-37T= XP_011528069.1:n.59-37T=
XM_011529768.2:c.59-37T= XP_011528070.1:n.59-37T=
XM_011529770.2:c.98-37T= XP_011528072.1:n.98-37T=
XM_017028487.1:c.-56-37T= XP_016883976.1:n.-56-37T=
XR_937576.2:n.324-37T=
NM_001001890.3:c.-21T= NP_001001890.1:n.-21T=
NM_001122607.2:c.-21T= NP_001116079.1:n.-21T=
NM_001754.5:c.98-37T= MANE Select NP_001745.2:n.98-37T=