Canonical Allele Identifier: CA410204234
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371567
ClinVar RCV Id: RCV001864583
dbSNP Id: rs2146414125

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887069G>T , CM000683.2:g.34887069G>T GRCh38
NC_000021.8:g.36259366G>T , CM000683.1:g.36259366G>T GRCh37
NC_000021.7:g.35181236G>T NCBI36
NG_011402.2:g.1102643C>A , LRG_482:g.1102643C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.125C>A MANE Select ENSP00000501943.1:p.Pro42Gln
ENST00000300305.7:c.125C>A ENSP00000300305.3:p.Pro42Gln
ENST00000344691.8:c.44C>A ENSP00000340690.4:p.Pro15Gln
ENST00000358356.9:c.44C>A ENSP00000351123.5:p.Pro15Gln
ENST00000399237.6:c.89C>A ENSP00000382182.2:p.Pro30Gln
ENST00000399240.5:c.44C>A ENSP00000382184.1:p.Pro15Gln
ENST00000437180.5:c.125C>A ENSP00000409227.1:p.Pro42Gln
ENST00000455571.5:c.86C>A ENSP00000388189.1:p.Pro29Gln
ENST00000475045.6:c.125C>A ENSP00000477072.1:p.Pro42Gln
ENST00000482318.5:c.59-6356C>A ENSP00000477067.1:n.59-6356C>A
NM_001001890.2:c.44C>A NP_001001890.1:p.Pro15Gln
NM_001122607.1:c.44C>A NP_001116079.1:p.Pro15Gln
NM_001754.4:c.125C>A , LRG_482t1:c.125C>A NP_001745.2:p.Pro42Gln
XM_005261068.3:c.89C>A XP_005261125.1:p.Pro30Gln
XM_005261069.3:c.125C>A XP_005261126.1:p.Pro42Gln
XM_011529766.1:c.125C>A XP_011528068.1:p.Pro42Gln
XM_011529767.1:c.86C>A XP_011528069.1:p.Pro29Gln
XM_011529768.1:c.86C>A XP_011528070.1:p.Pro29Gln
XM_011529770.1:c.125C>A XP_011528072.1:p.Pro42Gln
XR_937576.1:n.304C>A
XM_005261069.4:c.125C>A XP_005261126.1:p.Pro42Gln
XM_011529766.2:c.125C>A XP_011528068.1:p.Pro42Gln
XM_011529767.2:c.86C>A XP_011528069.1:p.Pro29Gln
XM_011529768.2:c.86C>A XP_011528070.1:p.Pro29Gln
XM_011529770.2:c.125C>A XP_011528072.1:p.Pro42Gln
XM_017028487.1:c.-29C>A XP_016883976.1:n.-29C>A
XR_937576.2:n.351C>A
NM_001001890.3:c.44C>A NP_001001890.1:p.Pro15Gln
NM_001122607.2:c.44C>A NP_001116079.1:p.Pro15Gln
NM_001754.5:c.125C>A MANE Select NP_001745.2:p.Pro42Gln