Canonical Allele Identifier: CA2580098649
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2024194
ClinVar RCV Id: RCV002863135

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880673_34880674insCGAT , CM000683.2:g.34880673_34880674insCGAT GRCh38
NC_000021.8:g.36252970_36252971insCGAT , CM000683.1:g.36252970_36252971insCGAT GRCh37
NC_000021.7:g.35174840_35174841insCGAT NCBI36
NG_011402.2:g.1109038_1109039insATCG , LRG_482:g.1109038_1109039insATCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.391_392insATCG MANE Select ENSP00000501943.1:p.Thr131AsnfsTer8
ENST00000300305.7:c.391_392insATCG ENSP00000300305.3:p.Thr131AsnfsTer8
ENST00000344691.8:c.310_311insATCG ENSP00000340690.4:p.Thr104AsnfsTer8
ENST00000358356.9:c.310_311insATCG ENSP00000351123.5:p.Thr104AsnfsTer8
ENST00000399237.6:c.355_356insATCG ENSP00000382182.2:p.Thr119AsnfsTer8
ENST00000399240.5:c.310_311insATCG ENSP00000382184.1:p.Thr104AsnfsTer8
ENST00000437180.5:c.391_392insATCG ENSP00000409227.1:p.Thr131AsnfsTer8
ENST00000455571.5:c.352_353insATCG ENSP00000388189.1:p.Thr118AsnfsTer8
ENST00000482318.5:c.98_99insATCG ENSP00000477067.1:p.His33GlnfsTer4
NM_001001890.2:c.310_311insATCG NP_001001890.1:p.Thr104AsnfsTer8
NM_001122607.1:c.310_311insATCG NP_001116079.1:p.Thr104AsnfsTer8
NM_001754.4:c.391_392insATCG , LRG_482t1:c.391_392insATCG NP_001745.2:p.Thr131AsnfsTer8
XM_005261068.3:c.355_356insATCG XP_005261125.1:p.Thr119AsnfsTer8
XM_005261069.3:c.391_392insATCG XP_005261126.1:p.Thr131AsnfsTer8
XM_011529766.1:c.391_392insATCG XP_011528068.1:p.Thr131AsnfsTer8
XM_011529767.1:c.352_353insATCG XP_011528069.1:p.Thr118AsnfsTer8
XM_011529768.1:c.352_353insATCG XP_011528070.1:p.Thr118AsnfsTer8
XM_011529770.1:c.391_392insATCG XP_011528072.1:p.Thr131AsnfsTer8
XR_937576.1:n.570_571insATCG
XM_005261069.4:c.391_392insATCG XP_005261126.1:p.Thr131AsnfsTer8
XM_011529766.2:c.391_392insATCG XP_011528068.1:p.Thr131AsnfsTer8
XM_011529767.2:c.352_353insATCG XP_011528069.1:p.Thr118AsnfsTer8
XM_011529768.2:c.352_353insATCG XP_011528070.1:p.Thr118AsnfsTer8
XM_011529770.2:c.391_392insATCG XP_011528072.1:p.Thr131AsnfsTer8
XM_017028487.1:c.238_239insATCG XP_016883976.1:p.Thr80AsnfsTer8
XR_937576.2:n.617_618insATCG
NM_001001890.3:c.310_311insATCG NP_001001890.1:p.Thr104AsnfsTer8
NM_001122607.2:c.310_311insATCG NP_001116079.1:p.Thr104AsnfsTer8
NM_001754.5:c.391_392insATCG MANE Select NP_001745.2:p.Thr131AsnfsTer8