Canonical Allele Identifier: CA2387294327
Gene: RUNX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880598G= , CM000683.2:g.34880598G= GRCh38
NC_000021.8:g.36252895G= , CM000683.1:g.36252895G= GRCh37
NC_000021.7:g.35174765G= NCBI36
NG_011402.2:g.1109114C= , LRG_482:g.1109114C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.467C= MANE Select ENSP00000501943.1:p.Ala156=
ENST00000300305.7:c.467C= ENSP00000300305.3:p.Ala156=
ENST00000344691.8:c.386C= ENSP00000340690.4:p.Ala129=
ENST00000358356.9:c.386C= ENSP00000351123.5:p.Ala129=
ENST00000399237.6:c.431C= ENSP00000382182.2:p.Ala144=
ENST00000399240.5:c.386C= ENSP00000382184.1:p.Ala129=
ENST00000437180.5:c.467C= ENSP00000409227.1:p.Ala156=
ENST00000482318.5:c.*57C= ENSP00000477067.1:n.*57C=
NM_001001890.2:c.386C= NP_001001890.1:p.Ala129=
NM_001122607.1:c.386C= NP_001116079.1:p.Ala129=
NM_001754.4:c.467C= , LRG_482t1:c.467C= NP_001745.2:p.Ala156=
XM_005261068.3:c.431C= XP_005261125.1:p.Ala144=
XM_005261069.3:c.467C= XP_005261126.1:p.Ala156=
XM_011529766.1:c.467C= XP_011528068.1:p.Ala156=
XM_011529767.1:c.428C= XP_011528069.1:p.Ala143=
XM_011529768.1:c.428C= XP_011528070.1:p.Ala143=
XM_011529770.1:c.467C= XP_011528072.1:p.Ala156=
XR_937576.1:n.646C=
XM_005261069.4:c.467C= XP_005261126.1:p.Ala156=
XM_011529766.2:c.467C= XP_011528068.1:p.Ala156=
XM_011529767.2:c.428C= XP_011528069.1:p.Ala143=
XM_011529768.2:c.428C= XP_011528070.1:p.Ala143=
XM_011529770.2:c.467C= XP_011528072.1:p.Ala156=
XM_017028487.1:c.314C= XP_016883976.1:p.Ala105=
XR_937576.2:n.693C=
NM_001001890.3:c.386C= NP_001001890.1:p.Ala129=
NM_001122607.2:c.386C= NP_001116079.1:p.Ala129=
NM_001754.5:c.467C= MANE Select NP_001745.2:p.Ala156=
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