Canonical Allele Identifier: CA645607345
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880572_34880573insT , CM000683.2:g.34880572_34880573insT GRCh38
NC_000021.8:g.36252869_36252870insT , CM000683.1:g.36252869_36252870insT GRCh37
NC_000021.7:g.35174739_35174740insT NCBI36
NG_011402.2:g.1109139_1109140insA , LRG_482:g.1109139_1109140insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.492_493insA MANE Select ENSP00000501943.1:p.Gly165ArgfsTer?
ENST00000300305.7:c.492_493insA ENSP00000300305.3:p.Gly165ArgfsTer?
ENST00000344691.8:c.411_412insA ENSP00000340690.4:p.Gly138ArgfsTer?
ENST00000358356.9:c.411_412insA ENSP00000351123.5:p.Gly138ArgfsTer?
ENST00000399237.6:c.456_457insA ENSP00000382182.2:p.Gly153ArgfsTer?
ENST00000399240.5:c.411_412insA ENSP00000382184.1:p.Gly138ArgfsTer?
ENST00000437180.5:c.492_493insA ENSP00000409227.1:p.Gly165ArgfsTer?
ENST00000482318.5:c.*82_*83insA ENSP00000477067.1:n.*82_*83insA
NM_001001890.2:c.411_412insA NP_001001890.1:p.Gly138ArgfsTer?
NM_001122607.1:c.411_412insA NP_001116079.1:p.Gly138ArgfsTer?
NM_001754.4:c.492_493insA , LRG_482t1:c.492_493insA NP_001745.2:p.Gly165ArgfsTer?
XM_005261068.3:c.456_457insA XP_005261125.1:p.Gly153ArgfsTer?
XM_005261069.3:c.492_493insA XP_005261126.1:p.Gly165ArgfsTer?
XM_011529766.1:c.492_493insA XP_011528068.1:p.Gly165ArgfsTer?
XM_011529767.1:c.453_454insA XP_011528069.1:p.Gly152ArgfsTer?
XM_011529768.1:c.453_454insA XP_011528070.1:p.Gly152ArgfsTer?
XM_011529770.1:c.492_493insA XP_011528072.1:p.Gly165ArgfsTer?
XR_937576.1:n.671_672insA
XM_005261069.4:c.492_493insA XP_005261126.1:p.Gly165ArgfsTer?
XM_011529766.2:c.492_493insA XP_011528068.1:p.Gly165ArgfsTer?
XM_011529767.2:c.453_454insA XP_011528069.1:p.Gly152ArgfsTer?
XM_011529768.2:c.453_454insA XP_011528070.1:p.Gly152ArgfsTer?
XM_011529770.2:c.492_493insA XP_011528072.1:p.Gly165ArgfsTer?
XM_017028487.1:c.339_340insA XP_016883976.1:p.Gly114ArgfsTer?
XR_937576.2:n.718_719insA
NM_001001890.3:c.411_412insA NP_001001890.1:p.Gly138ArgfsTer?
NM_001122607.2:c.411_412insA NP_001116079.1:p.Gly138ArgfsTer?
NM_001754.5:c.492_493insA MANE Select NP_001745.2:p.Gly165ArgfsTer?