Canonical Allele Identifier: CA410203672
Gene: RUNX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.36259205T>A (hg19) chr21:g.34886908T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886908T>A , CM000683.2:g.34886908T>A GRCh38
NC_000021.8:g.36259205T>A , CM000683.1:g.36259205T>A GRCh37
NC_000021.7:g.35181075T>A NCBI36
NG_011402.2:g.1102804A>T , LRG_482:g.1102804A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.286A>T MANE Select ENSP00000501943.1:p.Asn96Tyr
ENST00000300305.7:c.286A>T ENSP00000300305.3:p.Asn96Tyr
ENST00000344691.8:c.205A>T ENSP00000340690.4:p.Asn69Tyr
ENST00000358356.9:c.205A>T ENSP00000351123.5:p.Asn69Tyr
ENST00000399237.6:c.250A>T ENSP00000382182.2:p.Asn84Tyr
ENST00000399240.5:c.205A>T ENSP00000382184.1:p.Asn69Tyr
ENST00000437180.5:c.286A>T ENSP00000409227.1:p.Asn96Tyr
ENST00000455571.5:c.247A>T ENSP00000388189.1:p.Asn83Tyr
ENST00000482318.5:c.59-6195A>T ENSP00000477067.1:n.59-6195A>T
NM_001001890.2:c.205A>T NP_001001890.1:p.Asn69Tyr
NM_001122607.1:c.205A>T NP_001116079.1:p.Asn69Tyr
NM_001754.4:c.286A>T , LRG_482t1:c.286A>T NP_001745.2:p.Asn96Tyr
XM_005261068.3:c.250A>T XP_005261125.1:p.Asn84Tyr
XM_005261069.3:c.286A>T XP_005261126.1:p.Asn96Tyr
XM_011529766.1:c.286A>T XP_011528068.1:p.Asn96Tyr
XM_011529767.1:c.247A>T XP_011528069.1:p.Asn83Tyr
XM_011529768.1:c.247A>T XP_011528070.1:p.Asn83Tyr
XM_011529770.1:c.286A>T XP_011528072.1:p.Asn96Tyr
XR_937576.1:n.465A>T
XM_005261069.4:c.286A>T XP_005261126.1:p.Asn96Tyr
XM_011529766.2:c.286A>T XP_011528068.1:p.Asn96Tyr
XM_011529767.2:c.247A>T XP_011528069.1:p.Asn83Tyr
XM_011529768.2:c.247A>T XP_011528070.1:p.Asn83Tyr
XM_011529770.2:c.286A>T XP_011528072.1:p.Asn96Tyr
XM_017028487.1:c.133A>T XP_016883976.1:p.Asn45Tyr
XR_937576.2:n.512A>T
NM_001001890.3:c.205A>T NP_001001890.1:p.Asn69Tyr
NM_001122607.2:c.205A>T NP_001116079.1:p.Asn69Tyr
NM_001754.5:c.286A>T MANE Select NP_001745.2:p.Asn96Tyr
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