Canonical Allele Identifier: CA645607376
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880642_34880643insCCC , CM000683.2:g.34880642_34880643insCCC GRCh38
NC_000021.8:g.36252939_36252940insCCC , CM000683.1:g.36252939_36252940insCCC GRCh37
NC_000021.7:g.35174809_35174810insCCC NCBI36
NG_011402.2:g.1109071_1109072insGGG , LRG_482:g.1109071_1109072insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.424_425insGGG MANE Select ENSP00000501943.1:p.Ser141_Ala142insGly
ENST00000300305.7:c.424_425insGGG ENSP00000300305.3:p.Ser141_Ala142insGly
ENST00000344691.8:c.343_344insGGG ENSP00000340690.4:p.Ser114_Ala115insGly
ENST00000358356.9:c.343_344insGGG ENSP00000351123.5:p.Ser114_Ala115insGly
ENST00000399237.6:c.388_389insGGG ENSP00000382182.2:p.Ser129_Ala130insGly
ENST00000399240.5:c.343_344insGGG ENSP00000382184.1:p.Ser114_Ala115insGly
ENST00000437180.5:c.424_425insGGG ENSP00000409227.1:p.Ser141_Ala142insGly
ENST00000455571.5:c.385_386insGGG ENSP00000388189.1:p.Ser128_Ala129insGly
ENST00000482318.5:c.*14_*15insGGG ENSP00000477067.1:n.*14_*15insGGG
NM_001001890.2:c.343_344insGGG NP_001001890.1:p.Ser114_Ala115insGly
NM_001122607.1:c.343_344insGGG NP_001116079.1:p.Ser114_Ala115insGly
NM_001754.4:c.424_425insGGG , LRG_482t1:c.424_425insGGG NP_001745.2:p.Ser141_Ala142insGly
XM_005261068.3:c.388_389insGGG XP_005261125.1:p.Ser129_Ala130insGly
XM_005261069.3:c.424_425insGGG XP_005261126.1:p.Ser141_Ala142insGly
XM_011529766.1:c.424_425insGGG XP_011528068.1:p.Ser141_Ala142insGly
XM_011529767.1:c.385_386insGGG XP_011528069.1:p.Ser128_Ala129insGly
XM_011529768.1:c.385_386insGGG XP_011528070.1:p.Ser128_Ala129insGly
XM_011529770.1:c.424_425insGGG XP_011528072.1:p.Ser141_Ala142insGly
XR_937576.1:n.603_604insGGG
XM_005261069.4:c.424_425insGGG XP_005261126.1:p.Ser141_Ala142insGly
XM_011529766.2:c.424_425insGGG XP_011528068.1:p.Ser141_Ala142insGly
XM_011529767.2:c.385_386insGGG XP_011528069.1:p.Ser128_Ala129insGly
XM_011529768.2:c.385_386insGGG XP_011528070.1:p.Ser128_Ala129insGly
XM_011529770.2:c.424_425insGGG XP_011528072.1:p.Ser141_Ala142insGly
XM_017028487.1:c.271_272insGGG XP_016883976.1:p.Ser90_Ala91insGly
XR_937576.2:n.650_651insGGG
NM_001001890.3:c.343_344insGGG NP_001001890.1:p.Ser114_Ala115insGly
NM_001122607.2:c.343_344insGGG NP_001116079.1:p.Ser114_Ala115insGly
NM_001754.5:c.424_425insGGG MANE Select NP_001745.2:p.Ser141_Ala142insGly