Canonical Allele Identifier: CA2387294378
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880706_34880709delinsGCCA , CM000683.2:g.34880706_34880709delinsGCCA GRCh38
NC_000021.8:g.36253003_36253006delinsGCCA , CM000683.1:g.36253003_36253006delinsGCCA GRCh37
NC_000021.7:g.35174873_35174876delinsGCCA NCBI36
NG_011402.2:g.1109003_1109006delinsTGGC , LRG_482:g.1109003_1109006delinsTGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.356_359delinsTGGC MANE Select ENSP00000501943.1:p.Val119=
ENST00000300305.7:c.356_359delinsTGGC ENSP00000300305.3:p.Val119=
ENST00000344691.8:c.275_278delinsTGGC ENSP00000340690.4:p.Val92=
ENST00000358356.9:c.275_278delinsTGGC ENSP00000351123.5:p.Val92=
ENST00000399237.6:c.320_323delinsTGGC ENSP00000382182.2:p.Val107=
ENST00000399240.5:c.275_278delinsTGGC ENSP00000382184.1:p.Val92=
ENST00000437180.5:c.356_359delinsTGGC ENSP00000409227.1:p.Val119=
ENST00000455571.5:c.317_320delinsTGGC ENSP00000388189.1:p.Val106=
ENST00000482318.5:c.63_66delinsTGGC ENSP00000477067.1:p.Gly21=
NM_001001890.2:c.275_278delinsTGGC NP_001001890.1:p.Val92=
NM_001122607.1:c.275_278delinsTGGC NP_001116079.1:p.Val92=
NM_001754.4:c.356_359delinsTGGC , LRG_482t1:c.356_359delinsTGGC NP_001745.2:p.Val119=
XM_005261068.3:c.320_323delinsTGGC XP_005261125.1:p.Val107=
XM_005261069.3:c.356_359delinsTGGC XP_005261126.1:p.Val119=
XM_011529766.1:c.356_359delinsTGGC XP_011528068.1:p.Val119=
XM_011529767.1:c.317_320delinsTGGC XP_011528069.1:p.Val106=
XM_011529768.1:c.317_320delinsTGGC XP_011528070.1:p.Val106=
XM_011529770.1:c.356_359delinsTGGC XP_011528072.1:p.Val119=
XR_937576.1:n.535_538delinsTGGC
XM_005261069.4:c.356_359delinsTGGC XP_005261126.1:p.Val119=
XM_011529766.2:c.356_359delinsTGGC XP_011528068.1:p.Val119=
XM_011529767.2:c.317_320delinsTGGC XP_011528069.1:p.Val106=
XM_011529768.2:c.317_320delinsTGGC XP_011528070.1:p.Val106=
XM_011529770.2:c.356_359delinsTGGC XP_011528072.1:p.Val119=
XM_017028487.1:c.203_206delinsTGGC XP_016883976.1:p.Val68=
XR_937576.2:n.582_585delinsTGGC
NM_001001890.3:c.275_278delinsTGGC NP_001001890.1:p.Val92=
NM_001122607.2:c.275_278delinsTGGC NP_001116079.1:p.Val92=
NM_001754.5:c.356_359delinsTGGC MANE Select NP_001745.2:p.Val119=