Canonical Allele Identifier: CA637739332
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs1408379341

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886783G>C , CM000683.2:g.34886783G>C GRCh38
NC_000021.8:g.36259080G>C , CM000683.1:g.36259080G>C GRCh37
NC_000021.7:g.35180950G>C NCBI36
NG_011402.2:g.1102929C>G , LRG_482:g.1102929C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000675419.1:c.351+60C>G MANE Select ENSP00000501943.1:n.351+60C>G
ENST00000300305.7:c.351+60C>G ENSP00000300305.3:n.351+60C>G
ENST00000344691.8:c.270+60C>G ENSP00000340690.4:n.270+60C>G
ENST00000358356.9:c.270+60C>G ENSP00000351123.5:n.270+60C>G
ENST00000399237.6:c.315+60C>G ENSP00000382182.2:n.315+60C>G
ENST00000399240.5:c.270+60C>G ENSP00000382184.1:n.270+60C>G
ENST00000437180.5:c.351+60C>G ENSP00000409227.1:n.351+60C>G
ENST00000455571.5:c.312+60C>G ENSP00000388189.1:n.312+60C>G
ENST00000482318.5:c.59-6070C>G ENSP00000477067.1:n.59-6070C>G
NM_001001890.2:c.270+60C>G NP_001001890.1:n.270+60C>G
NM_001122607.1:c.270+60C>G NP_001116079.1:n.270+60C>G
NM_001754.4:c.351+60C>G , LRG_482t1:c.351+60C>G NP_001745.2:n.351+60C>G
XM_005261068.3:c.315+60C>G XP_005261125.1:n.315+60C>G
XM_005261069.3:c.351+60C>G XP_005261126.1:n.351+60C>G
XM_011529766.1:c.351+60C>G XP_011528068.1:n.351+60C>G
XM_011529767.1:c.312+60C>G XP_011528069.1:n.312+60C>G
XM_011529768.1:c.312+60C>G XP_011528070.1:n.312+60C>G
XM_011529770.1:c.351+60C>G XP_011528072.1:n.351+60C>G
XR_937576.1:n.530+60C>G
XM_005261069.4:c.351+60C>G XP_005261126.1:n.351+60C>G
XM_011529766.2:c.351+60C>G XP_011528068.1:n.351+60C>G
XM_011529767.2:c.312+60C>G XP_011528069.1:n.312+60C>G
XM_011529768.2:c.312+60C>G XP_011528070.1:n.312+60C>G
XM_011529770.2:c.351+60C>G XP_011528072.1:n.351+60C>G
XM_017028487.1:c.198+60C>G XP_016883976.1:n.198+60C>G
XR_937576.2:n.577+60C>G
NM_001001890.3:c.270+60C>G NP_001001890.1:n.270+60C>G
NM_001122607.2:c.270+60C>G NP_001116079.1:n.270+60C>G
NM_001754.5:c.351+60C>G MANE Select NP_001745.2:n.351+60C>G