Canonical Allele Identifier: CA2387301823
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34895185_34895186delinsAT , CM000683.2:g.34895185_34895186delinsAT GRCh38
NC_000021.8:g.36267482_36267483delinsAT , CM000683.1:g.36267482_36267483delinsAT GRCh37
NC_000021.7:g.35189352_35189353delinsAT NCBI36
NG_011402.2:g.1094526_1094527delinsAT , LRG_482:g.1094526_1094527delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.59-2223_59-2222delinsAT MANE Select ENSP00000501943.1:n.59-2223_59-2222delinsAT
ENST00000300305.7:c.59-2223_59-2222delinsAT ENSP00000300305.3:n.59-2223_59-2222delinsAT
ENST00000416754.1:c.59-2223_59-2222delinsAT ENSP00000405158.1:n.59-2223_59-2222delinsAT
ENST00000437180.5:c.59-2223_59-2222delinsAT ENSP00000409227.1:n.59-2223_59-2222delinsAT
ENST00000455571.5:c.59-8090_59-8089delinsAT ENSP00000388189.1:n.59-8090_59-8089delinsAT
ENST00000475045.6:c.59-2223_59-2222delinsAT ENSP00000477072.1:n.59-2223_59-2222delinsAT
ENST00000482318.5:c.59-14473_59-14472delinsAT ENSP00000477067.1:n.59-14473_59-14472delinsAT
NM_001754.4:c.59-2223_59-2222delinsAT , LRG_482t1:c.59-2223_59-2222delinsAT NP_001745.2:n.59-2223_59-2222delinsAT
XM_005261069.3:c.59-2223_59-2222delinsAT XP_005261126.1:n.59-2223_59-2222delinsAT
XM_011529766.1:c.59-2223_59-2222delinsAT XP_011528068.1:n.59-2223_59-2222delinsAT
XM_011529767.1:c.59-8090_59-8089delinsAT XP_011528069.1:n.59-8090_59-8089delinsAT
XM_011529768.1:c.59-8090_59-8089delinsAT XP_011528070.1:n.59-8090_59-8089delinsAT
XM_011529770.1:c.59-2223_59-2222delinsAT XP_011528072.1:n.59-2223_59-2222delinsAT
XR_937576.1:n.238-2223_238-2222delinsAT
XM_005261069.4:c.59-2223_59-2222delinsAT XP_005261126.1:n.59-2223_59-2222delinsAT
XM_011529766.2:c.59-2223_59-2222delinsAT XP_011528068.1:n.59-2223_59-2222delinsAT
XM_011529767.2:c.59-8090_59-8089delinsAT XP_011528069.1:n.59-8090_59-8089delinsAT
XM_011529768.2:c.59-8090_59-8089delinsAT XP_011528070.1:n.59-8090_59-8089delinsAT
XM_011529770.2:c.59-2223_59-2222delinsAT XP_011528072.1:n.59-2223_59-2222delinsAT
XR_937576.2:n.285-2223_285-2222delinsAT
NM_001754.5:c.59-2223_59-2222delinsAT MANE Select NP_001745.2:n.59-2223_59-2222delinsAT