Canonical Allele Identifier: CA1139771058
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34834577_34834578del , CM000683.2:g.34834577_34834578del GRCh38
NC_000021.8:g.36206874_36206875del , CM000683.1:g.36206874_36206875del GRCh37
NC_000021.7:g.35128744_35128745del NCBI36
NG_011402.2:g.1155134_1155135del , LRG_482:g.1155134_1155135del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.637_638del MANE Select ENSP00000501943.1:p.Gln213AspfsTer14
ENST00000300305.7:c.637_638del ENSP00000300305.3:p.Gln213AspfsTer14
ENST00000344691.8:c.556_557del ENSP00000340690.4:p.Gln186AspfsTer14
ENST00000358356.9:c.556_557del ENSP00000351123.5:p.Gln186AspfsTer14
ENST00000399237.6:c.601_602del ENSP00000382182.2:p.Gln201AspfsTer14
ENST00000399240.5:c.532+24896_532+24897del ENSP00000382184.1:n.532+24896_532+24897del
ENST00000437180.5:c.637_638del ENSP00000409227.1:p.Gln213AspfsTer14
ENST00000469087.1:n.173_174del
ENST00000482318.5:c.*227_*228del ENSP00000477067.1:n.*227_*228del
NM_001001890.2:c.556_557del NP_001001890.1:p.Gln186AspfsTer14
NM_001122607.1:c.556_557del NP_001116079.1:p.Gln186AspfsTer14
NM_001754.4:c.637_638del , LRG_482t1:c.637_638del NP_001745.2:p.Gln213AspfsTer14
XM_005261068.3:c.601_602del XP_005261125.1:p.Gln201AspfsTer14
XM_005261069.3:c.613+24896_613+24897del XP_005261126.1:n.613+24896_613+24897del
XM_011529766.1:c.637_638del XP_011528068.1:p.Gln213AspfsTer14
XM_011529767.1:c.598_599del XP_011528069.1:p.Gln200AspfsTer14
XM_011529768.1:c.574+24896_574+24897del XP_011528070.1:n.574+24896_574+24897del
XM_011529770.1:c.637_638del XP_011528072.1:p.Gln213AspfsTer14
XR_937576.1:n.816_817del
XM_005261069.4:c.613+24896_613+24897del XP_005261126.1:n.613+24896_613+24897del
XM_011529766.2:c.637_638del XP_011528068.1:p.Gln213AspfsTer14
XM_011529767.2:c.598_599del XP_011528069.1:p.Gln200AspfsTer14
XM_011529768.2:c.574+24896_574+24897del XP_011528070.1:n.574+24896_574+24897del
XM_011529770.2:c.637_638del XP_011528072.1:p.Gln213AspfsTer14
XM_017028487.1:c.484_485del XP_016883976.1:p.Gln162AspfsTer14
XR_937576.2:n.863_864del
NM_001001890.3:c.556_557del NP_001001890.1:p.Gln186AspfsTer14
NM_001122607.2:c.556_557del NP_001116079.1:p.Gln186AspfsTer14
NM_001754.5:c.637_638del MANE Select NP_001745.2:p.Gln213AspfsTer14