Canonical Allele Identifier: CA2518983303
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34895208del , CM000683.2:g.34895208del GRCh38
NC_000021.8:g.36267505del , CM000683.1:g.36267505del GRCh37
NC_000021.7:g.35189375del NCBI36
NG_011402.2:g.1094505del , LRG_482:g.1094505del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.59-2244del MANE Select ENSP00000501943.1:n.59-2244del
ENST00000300305.7:c.59-2244del ENSP00000300305.3:n.59-2244del
ENST00000416754.1:c.59-2244del ENSP00000405158.1:n.59-2244del
ENST00000437180.5:c.59-2244del ENSP00000409227.1:n.59-2244del
ENST00000455571.5:c.59-8111del ENSP00000388189.1:n.59-8111del
ENST00000475045.6:c.59-2244del ENSP00000477072.1:n.59-2244del
ENST00000482318.5:c.59-14494del ENSP00000477067.1:n.59-14494del
NM_001754.4:c.59-2244del , LRG_482t1:c.59-2244del NP_001745.2:n.59-2244del
XM_005261069.3:c.59-2244del XP_005261126.1:n.59-2244del
XM_011529766.1:c.59-2244del XP_011528068.1:n.59-2244del
XM_011529767.1:c.59-8111del XP_011528069.1:n.59-8111del
XM_011529768.1:c.59-8111del XP_011528070.1:n.59-8111del
XM_011529770.1:c.59-2244del XP_011528072.1:n.59-2244del
XR_937576.1:n.238-2244del
XM_005261069.4:c.59-2244del XP_005261126.1:n.59-2244del
XM_011529766.2:c.59-2244del XP_011528068.1:n.59-2244del
XM_011529767.2:c.59-8111del XP_011528069.1:n.59-8111del
XM_011529768.2:c.59-8111del XP_011528070.1:n.59-8111del
XM_011529770.2:c.59-2244del XP_011528072.1:n.59-2244del
XR_937576.2:n.285-2244del
NM_001754.5:c.59-2244del MANE Select NP_001745.2:n.59-2244del