Canonical Allele Identifier: CA2387297262
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887113_34887116delinsCACA , CM000683.2:g.34887113_34887116delinsCACA GRCh38
NC_000021.8:g.36259410_36259413delinsCACA , CM000683.1:g.36259410_36259413delinsCACA GRCh37
NC_000021.7:g.35181280_35181283delinsCACA NCBI36
NG_011402.2:g.1102596_1102599delinsTGTG , LRG_482:g.1102596_1102599delinsTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.98-20_98-17delinsTGTG MANE Select ENSP00000501943.1:n.98-20_98-17delinsTGTG
ENST00000300305.7:c.98-20_98-17delinsTGTG ENSP00000300305.3:n.98-20_98-17delinsTGTG
ENST00000344691.8:c.-4_-1delinsTGTG ENSP00000340690.4:n.-4_-1delinsTGTG
ENST00000358356.9:c.-4_-1delinsTGTG ENSP00000351123.5:n.-4_-1delinsTGTG
ENST00000399237.6:c.62-20_62-17delinsTGTG ENSP00000382182.2:n.62-20_62-17delinsTGTG
ENST00000399240.5:c.-4_-1delinsTGTG ENSP00000382184.1:n.-4_-1delinsTGTG
ENST00000437180.5:c.98-20_98-17delinsTGTG ENSP00000409227.1:n.98-20_98-17delinsTGTG
ENST00000455571.5:c.59-20_59-17delinsTGTG ENSP00000388189.1:n.59-20_59-17delinsTGTG
ENST00000475045.6:c.98-20_98-17delinsTGTG ENSP00000477072.1:n.98-20_98-17delinsTGTG
ENST00000482318.5:c.59-6403_59-6400delinsTGTG ENSP00000477067.1:n.59-6403_59-6400delinsTGTG
NM_001001890.2:c.-4_-1delinsTGTG NP_001001890.1:n.-4_-1delinsTGTG
NM_001122607.1:c.-4_-1delinsTGTG NP_001116079.1:n.-4_-1delinsTGTG
NM_001754.4:c.98-20_98-17delinsTGTG , LRG_482t1:c.98-20_98-17delinsTGTG NP_001745.2:n.98-20_98-17delinsTGTG
XM_005261068.3:c.62-20_62-17delinsTGTG XP_005261125.1:n.62-20_62-17delinsTGTG
XM_005261069.3:c.98-20_98-17delinsTGTG XP_005261126.1:n.98-20_98-17delinsTGTG
XM_011529766.1:c.98-20_98-17delinsTGTG XP_011528068.1:n.98-20_98-17delinsTGTG
XM_011529767.1:c.59-20_59-17delinsTGTG XP_011528069.1:n.59-20_59-17delinsTGTG
XM_011529768.1:c.59-20_59-17delinsTGTG XP_011528070.1:n.59-20_59-17delinsTGTG
XM_011529770.1:c.98-20_98-17delinsTGTG XP_011528072.1:n.98-20_98-17delinsTGTG
XR_937576.1:n.277-20_277-17delinsTGTG
XM_005261069.4:c.98-20_98-17delinsTGTG XP_005261126.1:n.98-20_98-17delinsTGTG
XM_011529766.2:c.98-20_98-17delinsTGTG XP_011528068.1:n.98-20_98-17delinsTGTG
XM_011529767.2:c.59-20_59-17delinsTGTG XP_011528069.1:n.59-20_59-17delinsTGTG
XM_011529768.2:c.59-20_59-17delinsTGTG XP_011528070.1:n.59-20_59-17delinsTGTG
XM_011529770.2:c.98-20_98-17delinsTGTG XP_011528072.1:n.98-20_98-17delinsTGTG
XM_017028487.1:c.-56-20_-56-17delinsTGTG XP_016883976.1:n.-56-20_-56-17delinsTGTG
XR_937576.2:n.324-20_324-17delinsTGTG
NM_001001890.3:c.-4_-1delinsTGTG NP_001001890.1:n.-4_-1delinsTGTG
NM_001122607.2:c.-4_-1delinsTGTG NP_001116079.1:n.-4_-1delinsTGTG
NM_001754.5:c.98-20_98-17delinsTGTG MANE Select NP_001745.2:n.98-20_98-17delinsTGTG