Canonical Allele Identifier: CA410202542
Gene: RUNX1 HGNC NCBI

Linked Data

dbSNP Id: rs2146361131
COSMIC: COSM5879748 COSM5879749
MyVariant Identifiers: chr21:g.36252890A>T (hg19) chr21:g.34880593A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880593A>T , CM000683.2:g.34880593A>T GRCh38
NC_000021.8:g.36252890A>T , CM000683.1:g.36252890A>T GRCh37
NC_000021.7:g.35174760A>T NCBI36
NG_011402.2:g.1109119T>A , LRG_482:g.1109119T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.472T>A MANE Select ENSP00000501943.1:p.Phe158Ile
ENST00000300305.7:c.472T>A ENSP00000300305.3:p.Phe158Ile
ENST00000344691.8:c.391T>A ENSP00000340690.4:p.Phe131Ile
ENST00000358356.9:c.391T>A ENSP00000351123.5:p.Phe131Ile
ENST00000399237.6:c.436T>A ENSP00000382182.2:p.Phe146Ile
ENST00000399240.5:c.391T>A ENSP00000382184.1:p.Phe131Ile
ENST00000437180.5:c.472T>A ENSP00000409227.1:p.Phe158Ile
ENST00000482318.5:c.*62T>A ENSP00000477067.1:n.*62T>A
NM_001001890.2:c.391T>A NP_001001890.1:p.Phe131Ile
NM_001122607.1:c.391T>A NP_001116079.1:p.Phe131Ile
NM_001754.4:c.472T>A , LRG_482t1:c.472T>A NP_001745.2:p.Phe158Ile
XM_005261068.3:c.436T>A XP_005261125.1:p.Phe146Ile
XM_005261069.3:c.472T>A XP_005261126.1:p.Phe158Ile
XM_011529766.1:c.472T>A XP_011528068.1:p.Phe158Ile
XM_011529767.1:c.433T>A XP_011528069.1:p.Phe145Ile
XM_011529768.1:c.433T>A XP_011528070.1:p.Phe145Ile
XM_011529770.1:c.472T>A XP_011528072.1:p.Phe158Ile
XR_937576.1:n.651T>A
XM_005261069.4:c.472T>A XP_005261126.1:p.Phe158Ile
XM_011529766.2:c.472T>A XP_011528068.1:p.Phe158Ile
XM_011529767.2:c.433T>A XP_011528069.1:p.Phe145Ile
XM_011529768.2:c.433T>A XP_011528070.1:p.Phe145Ile
XM_011529770.2:c.472T>A XP_011528072.1:p.Phe158Ile
XM_017028487.1:c.319T>A XP_016883976.1:p.Phe107Ile
XR_937576.2:n.698T>A
NM_001001890.3:c.391T>A NP_001001890.1:p.Phe131Ile
NM_001122607.2:c.391T>A NP_001116079.1:p.Phe131Ile
NM_001754.5:c.472T>A MANE Select NP_001745.2:p.Phe158Ile
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