Canonical Allele Identifier: CA410202790
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439732
ClinVar RCV Id: RCV001936692
dbSNP Id: rs2057890361

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880713C>A , CM000683.2:g.34880713C>A GRCh38
NC_000021.8:g.36253010C>A , CM000683.1:g.36253010C>A GRCh37
NC_000021.7:g.35174880C>A NCBI36
NG_011402.2:g.1108999G>T , LRG_482:g.1108999G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.352G>T MANE Select ENSP00000501943.1:p.Val118Leu
ENST00000300305.7:c.352G>T ENSP00000300305.3:p.Val118Leu
ENST00000344691.8:c.271G>T ENSP00000340690.4:p.Val91Leu
ENST00000358356.9:c.271G>T ENSP00000351123.5:p.Val91Leu
ENST00000399237.6:c.316G>T ENSP00000382182.2:p.Val106Leu
ENST00000399240.5:c.271G>T ENSP00000382184.1:p.Val91Leu
ENST00000437180.5:c.352G>T ENSP00000409227.1:p.Val118Leu
ENST00000455571.5:c.313G>T ENSP00000388189.1:p.Val105Leu
ENST00000482318.5:c.59G>T ENSP00000477067.1:p.Gly20Val
NM_001001890.2:c.271G>T NP_001001890.1:p.Val91Leu
NM_001122607.1:c.271G>T NP_001116079.1:p.Val91Leu
NM_001754.4:c.352G>T , LRG_482t1:c.352G>T NP_001745.2:p.Val118Leu
XM_005261068.3:c.316G>T XP_005261125.1:p.Val106Leu
XM_005261069.3:c.352G>T XP_005261126.1:p.Val118Leu
XM_011529766.1:c.352G>T XP_011528068.1:p.Val118Leu
XM_011529767.1:c.313G>T XP_011528069.1:p.Val105Leu
XM_011529768.1:c.313G>T XP_011528070.1:p.Val105Leu
XM_011529770.1:c.352G>T XP_011528072.1:p.Val118Leu
XR_937576.1:n.531G>T
XM_005261069.4:c.352G>T XP_005261126.1:p.Val118Leu
XM_011529766.2:c.352G>T XP_011528068.1:p.Val118Leu
XM_011529767.2:c.313G>T XP_011528069.1:p.Val105Leu
XM_011529768.2:c.313G>T XP_011528070.1:p.Val105Leu
XM_011529770.2:c.352G>T XP_011528072.1:p.Val118Leu
XM_017028487.1:c.199G>T XP_016883976.1:p.Val67Leu
XR_937576.2:n.578G>T
NM_001001890.3:c.271G>T NP_001001890.1:p.Val91Leu
NM_001122607.2:c.271G>T NP_001116079.1:p.Val91Leu
NM_001754.5:c.352G>T MANE Select NP_001745.2:p.Val118Leu