Canonical Allele Identifier: CA645607342
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM25139

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880573delinsTCCT , CM000683.2:g.34880573delinsTCCT GRCh38
NC_000021.8:g.36252870delinsTCCT , CM000683.1:g.36252870delinsTCCT GRCh37
NC_000021.7:g.35174740delinsTCCT NCBI36
NG_011402.2:g.1109139delinsAGGA , LRG_482:g.1109139delinsAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.492delinsAGGA MANE Select ENSP00000501943.1:p.Val164_Gly165insGly
ENST00000300305.7:c.492delinsAGGA ENSP00000300305.3:p.Val164_Gly165insGly
ENST00000344691.8:c.411delinsAGGA ENSP00000340690.4:p.Val137_Gly138insGly
ENST00000358356.9:c.411delinsAGGA ENSP00000351123.5:p.Val137_Gly138insGly
ENST00000399237.6:c.456delinsAGGA ENSP00000382182.2:p.Val152_Gly153insGly
ENST00000399240.5:c.411delinsAGGA ENSP00000382184.1:p.Val137_Gly138insGly
ENST00000437180.5:c.492delinsAGGA ENSP00000409227.1:p.Val164_Gly165insGly
ENST00000482318.5:c.*82delinsAGGA ENSP00000477067.1:n.*82delinsAGGA
NM_001001890.2:c.411delinsAGGA NP_001001890.1:p.Val137_Gly138insGly
NM_001122607.1:c.411delinsAGGA NP_001116079.1:p.Val137_Gly138insGly
NM_001754.4:c.492delinsAGGA , LRG_482t1:c.492delinsAGGA NP_001745.2:p.Val164_Gly165insGly
XM_005261068.3:c.456delinsAGGA XP_005261125.1:p.Val152_Gly153insGly
XM_005261069.3:c.492delinsAGGA XP_005261126.1:p.Val164_Gly165insGly
XM_011529766.1:c.492delinsAGGA XP_011528068.1:p.Val164_Gly165insGly
XM_011529767.1:c.453delinsAGGA XP_011528069.1:p.Val151_Gly152insGly
XM_011529768.1:c.453delinsAGGA XP_011528070.1:p.Val151_Gly152insGly
XM_011529770.1:c.492delinsAGGA XP_011528072.1:p.Val164_Gly165insGly
XR_937576.1:n.671delinsAGGA
XM_005261069.4:c.492delinsAGGA XP_005261126.1:p.Val164_Gly165insGly
XM_011529766.2:c.492delinsAGGA XP_011528068.1:p.Val164_Gly165insGly
XM_011529767.2:c.453delinsAGGA XP_011528069.1:p.Val151_Gly152insGly
XM_011529768.2:c.453delinsAGGA XP_011528070.1:p.Val151_Gly152insGly
XM_011529770.2:c.492delinsAGGA XP_011528072.1:p.Val164_Gly165insGly
XM_017028487.1:c.339delinsAGGA XP_016883976.1:p.Val113_Gly114insGly
XR_937576.2:n.718delinsAGGA
NM_001001890.3:c.411delinsAGGA NP_001001890.1:p.Val137_Gly138insGly
NM_001122607.2:c.411delinsAGGA NP_001116079.1:p.Val137_Gly138insGly
NM_001754.5:c.492delinsAGGA MANE Select NP_001745.2:p.Val164_Gly165insGly