Canonical Allele Identifier: CA645607333
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880572_34880575dup , CM000683.2:g.34880572_34880575dup GRCh38
NC_000021.8:g.36252869_36252872dup , CM000683.1:g.36252869_36252872dup GRCh37
NC_000021.7:g.35174739_35174742dup NCBI36
NG_011402.2:g.1109141_1109144dup , LRG_482:g.1109141_1109144dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.494_497dup MANE Select ENSP00000501943.1:p.Gly168LysfsTer?
ENST00000300305.7:c.494_497dup ENSP00000300305.3:p.Gly168LysfsTer?
ENST00000344691.8:c.413_416dup ENSP00000340690.4:p.Gly141LysfsTer?
ENST00000358356.9:c.413_416dup ENSP00000351123.5:p.Gly141LysfsTer?
ENST00000399237.6:c.458_461dup ENSP00000382182.2:p.Gly156LysfsTer?
ENST00000399240.5:c.413_416dup ENSP00000382184.1:p.Gly141LysfsTer?
ENST00000437180.5:c.494_497dup ENSP00000409227.1:p.Gly168LysfsTer?
ENST00000482318.5:c.*84_*87dup ENSP00000477067.1:n.*84_*87dup
NM_001001890.2:c.413_416dup NP_001001890.1:p.Gly141LysfsTer?
NM_001122607.1:c.413_416dup NP_001116079.1:p.Gly141LysfsTer?
NM_001754.4:c.494_497dup , LRG_482t1:c.494_497dup NP_001745.2:p.Gly168LysfsTer?
XM_005261068.3:c.458_461dup XP_005261125.1:p.Gly156LysfsTer?
XM_005261069.3:c.494_497dup XP_005261126.1:p.Gly168LysfsTer?
XM_011529766.1:c.494_497dup XP_011528068.1:p.Gly168LysfsTer?
XM_011529767.1:c.455_458dup XP_011528069.1:p.Gly155LysfsTer?
XM_011529768.1:c.455_458dup XP_011528070.1:p.Gly155LysfsTer?
XM_011529770.1:c.494_497dup XP_011528072.1:p.Gly168LysfsTer?
XR_937576.1:n.673_676dup
XM_005261069.4:c.494_497dup XP_005261126.1:p.Gly168LysfsTer?
XM_011529766.2:c.494_497dup XP_011528068.1:p.Gly168LysfsTer?
XM_011529767.2:c.455_458dup XP_011528069.1:p.Gly155LysfsTer?
XM_011529768.2:c.455_458dup XP_011528070.1:p.Gly155LysfsTer?
XM_011529770.2:c.494_497dup XP_011528072.1:p.Gly168LysfsTer?
XM_017028487.1:c.341_344dup XP_016883976.1:p.Gly117LysfsTer?
XR_937576.2:n.720_723dup
NM_001001890.3:c.413_416dup NP_001001890.1:p.Gly141LysfsTer?
NM_001122607.2:c.413_416dup NP_001116079.1:p.Gly141LysfsTer?
NM_001754.5:c.494_497dup MANE Select NP_001745.2:p.Gly168LysfsTer?