Canonical Allele Identifier: CA2580098648
Gene: RUNX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2092471
ClinVar RCV Id: RCV002996576

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880671_34880681del , CM000683.2:g.34880671_34880681del GRCh38
NC_000021.8:g.36252968_36252978del , CM000683.1:g.36252968_36252978del GRCh37
NC_000021.7:g.35174838_35174848del NCBI36
NG_011402.2:g.1109032_1109042del , LRG_482:g.1109032_1109042del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.385_395del MANE Select ENSP00000501943.1:p.Leu129AspfsTer5
ENST00000300305.7:c.385_395del ENSP00000300305.3:p.Leu129AspfsTer5
ENST00000344691.8:c.304_314del ENSP00000340690.4:p.Leu102AspfsTer5
ENST00000358356.9:c.304_314del ENSP00000351123.5:p.Leu102AspfsTer5
ENST00000399237.6:c.349_359del ENSP00000382182.2:p.Leu117AspfsTer5
ENST00000399240.5:c.304_314del ENSP00000382184.1:p.Leu102AspfsTer5
ENST00000437180.5:c.385_395del ENSP00000409227.1:p.Leu129AspfsTer5
ENST00000455571.5:c.346_356del ENSP00000388189.1:p.Leu116AspfsTer5
ENST00000482318.5:c.92_102del ENSP00000477067.1:p.Ser31Ter
NM_001001890.2:c.304_314del NP_001001890.1:p.Leu102AspfsTer5
NM_001122607.1:c.304_314del NP_001116079.1:p.Leu102AspfsTer5
NM_001754.4:c.385_395del , LRG_482t1:c.385_395del NP_001745.2:p.Leu129AspfsTer5
XM_005261068.3:c.349_359del XP_005261125.1:p.Leu117AspfsTer5
XM_005261069.3:c.385_395del XP_005261126.1:p.Leu129AspfsTer5
XM_011529766.1:c.385_395del XP_011528068.1:p.Leu129AspfsTer5
XM_011529767.1:c.346_356del XP_011528069.1:p.Leu116AspfsTer5
XM_011529768.1:c.346_356del XP_011528070.1:p.Leu116AspfsTer5
XM_011529770.1:c.385_395del XP_011528072.1:p.Leu129AspfsTer5
XR_937576.1:n.564_574del
XM_005261069.4:c.385_395del XP_005261126.1:p.Leu129AspfsTer5
XM_011529766.2:c.385_395del XP_011528068.1:p.Leu129AspfsTer5
XM_011529767.2:c.346_356del XP_011528069.1:p.Leu116AspfsTer5
XM_011529768.2:c.346_356del XP_011528070.1:p.Leu116AspfsTer5
XM_011529770.2:c.385_395del XP_011528072.1:p.Leu129AspfsTer5
XM_017028487.1:c.232_242del XP_016883976.1:p.Leu78AspfsTer5
XR_937576.2:n.611_621del
NM_001001890.3:c.304_314del NP_001001890.1:p.Leu102AspfsTer5
NM_001122607.2:c.304_314del NP_001116079.1:p.Leu102AspfsTer5
NM_001754.5:c.385_395del MANE Select NP_001745.2:p.Leu129AspfsTer5