Canonical Allele Identifier: CA2654380110
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880408_34880409insGT , CM000683.2:g.34880408_34880409insGT GRCh38
NC_000021.8:g.36252705_36252706insGT , CM000683.1:g.36252705_36252706insGT GRCh37
NC_000021.7:g.35174575_35174576insGT NCBI36
NG_011402.2:g.1109303_1109304insAC , LRG_482:g.1109303_1109304insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.508+148_508+149insAC MANE Select ENSP00000501943.1:n.508+148_508+149insAC
ENST00000300305.7:c.508+148_508+149insAC ENSP00000300305.3:n.508+148_508+149insAC
ENST00000344691.8:c.427+148_427+149insAC ENSP00000340690.4:n.427+148_427+149insAC
ENST00000358356.9:c.427+148_427+149insAC ENSP00000351123.5:n.427+148_427+149insAC
ENST00000399237.6:c.472+148_472+149insAC ENSP00000382182.2:n.472+148_472+149insAC
ENST00000399240.5:c.427+148_427+149insAC ENSP00000382184.1:n.427+148_427+149insAC
ENST00000437180.5:c.508+148_508+149insAC ENSP00000409227.1:n.508+148_508+149insAC
ENST00000482318.5:c.*98+148_*98+149insAC ENSP00000477067.1:n.*98+148_*98+149insAC
NM_001001890.2:c.427+148_427+149insAC NP_001001890.1:n.427+148_427+149insAC
NM_001122607.1:c.427+148_427+149insAC NP_001116079.1:n.427+148_427+149insAC
NM_001754.4:c.508+148_508+149insAC , LRG_482t1:c.508+148_508+149insAC NP_001745.2:n.508+148_508+149insAC
XM_005261068.3:c.472+148_472+149insAC XP_005261125.1:n.472+148_472+149insAC
XM_005261069.3:c.508+148_508+149insAC XP_005261126.1:n.508+148_508+149insAC
XM_011529766.1:c.508+148_508+149insAC XP_011528068.1:n.508+148_508+149insAC
XM_011529767.1:c.469+148_469+149insAC XP_011528069.1:n.469+148_469+149insAC
XM_011529768.1:c.469+148_469+149insAC XP_011528070.1:n.469+148_469+149insAC
XM_011529770.1:c.508+148_508+149insAC XP_011528072.1:n.508+148_508+149insAC
XR_937576.1:n.687+148_687+149insAC
XM_005261069.4:c.508+148_508+149insAC XP_005261126.1:n.508+148_508+149insAC
XM_011529766.2:c.508+148_508+149insAC XP_011528068.1:n.508+148_508+149insAC
XM_011529767.2:c.469+148_469+149insAC XP_011528069.1:n.469+148_469+149insAC
XM_011529768.2:c.469+148_469+149insAC XP_011528070.1:n.469+148_469+149insAC
XM_011529770.2:c.508+148_508+149insAC XP_011528072.1:n.508+148_508+149insAC
XM_017028487.1:c.355+148_355+149insAC XP_016883976.1:n.355+148_355+149insAC
XR_937576.2:n.734+148_734+149insAC
NM_001001890.3:c.427+148_427+149insAC NP_001001890.1:n.427+148_427+149insAC
NM_001122607.2:c.427+148_427+149insAC NP_001116079.1:n.427+148_427+149insAC
NM_001754.5:c.508+148_508+149insAC MANE Select NP_001745.2:n.508+148_508+149insAC