Canonical Allele Identifier: CA2387294309
Gene: RUNX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880562C= , CM000683.2:g.34880562C= GRCh38
NC_000021.8:g.36252859C= , CM000683.1:g.36252859C= GRCh37
NC_000021.7:g.35174729C= NCBI36
NG_011402.2:g.1109150G= , LRG_482:g.1109150G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.503G= MANE Select ENSP00000501943.1:p.Gly168=
ENST00000300305.7:c.503G= ENSP00000300305.3:p.Gly168=
ENST00000344691.8:c.422G= ENSP00000340690.4:p.Gly141=
ENST00000358356.9:c.422G= ENSP00000351123.5:p.Gly141=
ENST00000399237.6:c.467G= ENSP00000382182.2:p.Gly156=
ENST00000399240.5:c.422G= ENSP00000382184.1:p.Gly141=
ENST00000437180.5:c.503G= ENSP00000409227.1:p.Gly168=
ENST00000482318.5:c.*93G= ENSP00000477067.1:n.*93G=
NM_001001890.2:c.422G= NP_001001890.1:p.Gly141=
NM_001122607.1:c.422G= NP_001116079.1:p.Gly141=
NM_001754.4:c.503G= , LRG_482t1:c.503G= NP_001745.2:p.Gly168=
XM_005261068.3:c.467G= XP_005261125.1:p.Gly156=
XM_005261069.3:c.503G= XP_005261126.1:p.Gly168=
XM_011529766.1:c.503G= XP_011528068.1:p.Gly168=
XM_011529767.1:c.464G= XP_011528069.1:p.Gly155=
XM_011529768.1:c.464G= XP_011528070.1:p.Gly155=
XM_011529770.1:c.503G= XP_011528072.1:p.Gly168=
XR_937576.1:n.682G=
XM_005261069.4:c.503G= XP_005261126.1:p.Gly168=
XM_011529766.2:c.503G= XP_011528068.1:p.Gly168=
XM_011529767.2:c.464G= XP_011528069.1:p.Gly155=
XM_011529768.2:c.464G= XP_011528070.1:p.Gly155=
XM_011529770.2:c.503G= XP_011528072.1:p.Gly168=
XM_017028487.1:c.350G= XP_016883976.1:p.Gly117=
XR_937576.2:n.729G=
NM_001001890.3:c.422G= NP_001001890.1:p.Gly141=
NM_001122607.2:c.422G= NP_001116079.1:p.Gly141=
NM_001754.5:c.503G= MANE Select NP_001745.2:p.Gly168=
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