Canonical Allele Identifier: CA2695230131
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886877_34886878delinsAT , CM000683.2:g.34886877_34886878delinsAT GRCh38
NC_000021.8:g.36259174_36259175delinsAT , CM000683.1:g.36259174_36259175delinsAT GRCh37
NC_000021.7:g.35181044_35181045delinsAT NCBI36
NG_011402.2:g.1102834_1102835delinsAT , LRG_482:g.1102834_1102835delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.316_317delinsAT MANE Select ENSP00000501943.1:p.Trp106Met
ENST00000300305.7:c.316_317delinsAT ENSP00000300305.3:p.Trp106Met
ENST00000344691.8:c.235_236delinsAT ENSP00000340690.4:p.Trp79Met
ENST00000358356.9:c.235_236delinsAT ENSP00000351123.5:p.Trp79Met
ENST00000399237.6:c.280_281delinsAT ENSP00000382182.2:p.Trp94Met
ENST00000399240.5:c.235_236delinsAT ENSP00000382184.1:p.Trp79Met
ENST00000437180.5:c.316_317delinsAT ENSP00000409227.1:p.Trp106Met
ENST00000455571.5:c.277_278delinsAT ENSP00000388189.1:p.Trp93Met
ENST00000482318.5:c.59-6165_59-6164delinsAT ENSP00000477067.1:n.59-6165_59-6164delinsAT
NM_001001890.2:c.235_236delinsAT NP_001001890.1:p.Trp79Met
NM_001122607.1:c.235_236delinsAT NP_001116079.1:p.Trp79Met
NM_001754.4:c.316_317delinsAT , LRG_482t1:c.316_317delinsAT NP_001745.2:p.Trp106Met
XM_005261068.3:c.280_281delinsAT XP_005261125.1:p.Trp94Met
XM_005261069.3:c.316_317delinsAT XP_005261126.1:p.Trp106Met
XM_011529766.1:c.316_317delinsAT XP_011528068.1:p.Trp106Met
XM_011529767.1:c.277_278delinsAT XP_011528069.1:p.Trp93Met
XM_011529768.1:c.277_278delinsAT XP_011528070.1:p.Trp93Met
XM_011529770.1:c.316_317delinsAT XP_011528072.1:p.Trp106Met
XR_937576.1:n.495_496delinsAT
XM_005261069.4:c.316_317delinsAT XP_005261126.1:p.Trp106Met
XM_011529766.2:c.316_317delinsAT XP_011528068.1:p.Trp106Met
XM_011529767.2:c.277_278delinsAT XP_011528069.1:p.Trp93Met
XM_011529768.2:c.277_278delinsAT XP_011528070.1:p.Trp93Met
XM_011529770.2:c.316_317delinsAT XP_011528072.1:p.Trp106Met
XM_017028487.1:c.163_164delinsAT XP_016883976.1:p.Trp55Met
XR_937576.2:n.542_543delinsAT
NM_001001890.3:c.235_236delinsAT NP_001001890.1:p.Trp79Met
NM_001122607.2:c.235_236delinsAT NP_001116079.1:p.Trp79Met
NM_001754.5:c.316_317delinsAT MANE Select NP_001745.2:p.Trp106Met