Canonical Allele Identifier: CA410203349
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1438740
ClinVar RCV Id: RCV001965248
dbSNP Id: rs2146407735

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886845T>C , CM000683.2:g.34886845T>C GRCh38
NC_000021.8:g.36259142T>C , CM000683.1:g.36259142T>C GRCh37
NC_000021.7:g.35181012T>C NCBI36
NG_011402.2:g.1102867A>G , LRG_482:g.1102867A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.349A>G MANE Select ENSP00000501943.1:p.Lys117Glu
ENST00000300305.7:c.349A>G ENSP00000300305.3:p.Lys117Glu
ENST00000344691.8:c.268A>G ENSP00000340690.4:p.Lys90Glu
ENST00000358356.9:c.268A>G ENSP00000351123.5:p.Lys90Glu
ENST00000399237.6:c.313A>G ENSP00000382182.2:p.Lys105Glu
ENST00000399240.5:c.268A>G ENSP00000382184.1:p.Lys90Glu
ENST00000437180.5:c.349A>G ENSP00000409227.1:p.Lys117Glu
ENST00000455571.5:c.310A>G ENSP00000388189.1:p.Lys104Glu
ENST00000482318.5:c.59-6132A>G ENSP00000477067.1:n.59-6132A>G
NM_001001890.2:c.268A>G NP_001001890.1:p.Lys90Glu
NM_001122607.1:c.268A>G NP_001116079.1:p.Lys90Glu
NM_001754.4:c.349A>G , LRG_482t1:c.349A>G NP_001745.2:p.Lys117Glu
XM_005261068.3:c.313A>G XP_005261125.1:p.Lys105Glu
XM_005261069.3:c.349A>G XP_005261126.1:p.Lys117Glu
XM_011529766.1:c.349A>G XP_011528068.1:p.Lys117Glu
XM_011529767.1:c.310A>G XP_011528069.1:p.Lys104Glu
XM_011529768.1:c.310A>G XP_011528070.1:p.Lys104Glu
XM_011529770.1:c.349A>G XP_011528072.1:p.Lys117Glu
XR_937576.1:n.528A>G
XM_005261069.4:c.349A>G XP_005261126.1:p.Lys117Glu
XM_011529766.2:c.349A>G XP_011528068.1:p.Lys117Glu
XM_011529767.2:c.310A>G XP_011528069.1:p.Lys104Glu
XM_011529768.2:c.310A>G XP_011528070.1:p.Lys104Glu
XM_011529770.2:c.349A>G XP_011528072.1:p.Lys117Glu
XM_017028487.1:c.196A>G XP_016883976.1:p.Lys66Glu
XR_937576.2:n.575A>G
NM_001001890.3:c.268A>G NP_001001890.1:p.Lys90Glu
NM_001122607.2:c.268A>G NP_001116079.1:p.Lys90Glu
NM_001754.5:c.349A>G MANE Select NP_001745.2:p.Lys117Glu