Canonical Allele Identifier: CA645608302
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34859486_34859487delinsAA , CM000683.2:g.34859486_34859487delinsAA GRCh38
NC_000021.8:g.36231783_36231784delinsAA , CM000683.1:g.36231783_36231784delinsAA GRCh37
NC_000021.7:g.35153653_35153654delinsAA NCBI36
NG_011402.2:g.1130225_1130226delinsTT , LRG_482:g.1130225_1130226delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.600_601delinsTT MANE Select ENSP00000501943.1:p.Pro201Ter
ENST00000300305.7:c.600_601delinsTT ENSP00000300305.3:p.Pro201Ter
ENST00000344691.8:c.519_520delinsTT ENSP00000340690.4:p.Pro174Ter
ENST00000358356.9:c.519_520delinsTT ENSP00000351123.5:p.Pro174Ter
ENST00000399237.6:c.564_565delinsTT ENSP00000382182.2:p.Pro189Ter
ENST00000399240.5:c.519_520delinsTT ENSP00000382184.1:p.Pro174Ter
ENST00000437180.5:c.600_601delinsTT ENSP00000409227.1:p.Pro201Ter
ENST00000467577.1:n.92_93delinsTT
ENST00000482318.5:c.*190_*191delinsTT ENSP00000477067.1:n.*190_*191delinsTT
NM_001001890.2:c.519_520delinsTT NP_001001890.1:p.Pro174Ter
NM_001122607.1:c.519_520delinsTT NP_001116079.1:p.Pro174Ter
NM_001754.4:c.600_601delinsTT , LRG_482t1:c.600_601delinsTT NP_001745.2:p.Pro201Ter
XM_005261068.3:c.564_565delinsTT XP_005261125.1:p.Pro189Ter
XM_005261069.3:c.600_601delinsTT XP_005261126.1:p.Pro201Ter
XM_011529766.1:c.600_601delinsTT XP_011528068.1:p.Pro201Ter
XM_011529767.1:c.561_562delinsTT XP_011528069.1:p.Pro188Ter
XM_011529768.1:c.561_562delinsTT XP_011528070.1:p.Pro188Ter
XM_011529770.1:c.600_601delinsTT XP_011528072.1:p.Pro201Ter
XR_937576.1:n.779_780delinsTT
XM_005261069.4:c.600_601delinsTT XP_005261126.1:p.Pro201Ter
XM_011529766.2:c.600_601delinsTT XP_011528068.1:p.Pro201Ter
XM_011529767.2:c.561_562delinsTT XP_011528069.1:p.Pro188Ter
XM_011529768.2:c.561_562delinsTT XP_011528070.1:p.Pro188Ter
XM_011529770.2:c.600_601delinsTT XP_011528072.1:p.Pro201Ter
XM_017028487.1:c.447_448delinsTT XP_016883976.1:p.Pro150Ter
XR_937576.2:n.826_827delinsTT
NM_001001890.3:c.519_520delinsTT NP_001001890.1:p.Pro174Ter
NM_001122607.2:c.519_520delinsTT NP_001116079.1:p.Pro174Ter
NM_001754.5:c.600_601delinsTT MANE Select NP_001745.2:p.Pro201Ter