Canonical Allele Identifier: CA645607323
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM5879729 COSM5879730
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880570_34880571insGGAAAGCCACTTCGA , CM000683.2:g.34880570_34880571insGGAAAGCCACTTCGA GRCh38
NC_000021.8:g.36252867_36252868insGGAAAGCCACTTCGA , CM000683.1:g.36252867_36252868insGGAAAGCCACTTCGA GRCh37
NC_000021.7:g.35174737_35174738insGGAAAGCCACTTCGA NCBI36
NG_011402.2:g.1109150_1109151insCTTTCCTCGAAGTGG , LRG_482:g.1109150_1109151insCTTTCCTCGAAGTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.503_504insCTTTCCTCGAAGTGG MANE Select ENSP00000501943.1:p.Gly168_Arg169insPheProArgSerGly
ENST00000300305.7:c.503_504insCTTTCCTCGAAGTGG ENSP00000300305.3:p.Gly168_Arg169insPheProArgSerGly
ENST00000344691.8:c.422_423insCTTTCCTCGAAGTGG ENSP00000340690.4:p.Gly141_Arg142insPheProArgSerGly
ENST00000358356.9:c.422_423insCTTTCCTCGAAGTGG ENSP00000351123.5:p.Gly141_Arg142insPheProArgSerGly
ENST00000399237.6:c.467_468insCTTTCCTCGAAGTGG ENSP00000382182.2:p.Gly156_Arg157insPheProArgSerGly
ENST00000399240.5:c.422_423insCTTTCCTCGAAGTGG ENSP00000382184.1:p.Gly141_Arg142insPheProArgSerGly
ENST00000437180.5:c.503_504insCTTTCCTCGAAGTGG ENSP00000409227.1:p.Gly168_Arg169insPheProArgSerGly
ENST00000482318.5:c.*93_*94insCTTTCCTCGAAGTGG ENSP00000477067.1:n.*93_*94insCTTTCCTCGAAGTGG
NM_001001890.2:c.422_423insCTTTCCTCGAAGTGG NP_001001890.1:p.Gly141_Arg142insPheProArgSerGly
NM_001122607.1:c.422_423insCTTTCCTCGAAGTGG NP_001116079.1:p.Gly141_Arg142insPheProArgSerGly
NM_001754.4:c.503_504insCTTTCCTCGAAGTGG , LRG_482t1:c.503_504insCTTTCCTCGAAGTGG NP_001745.2:p.Gly168_Arg169insPheProArgSerGly
XM_005261068.3:c.467_468insCTTTCCTCGAAGTGG XP_005261125.1:p.Gly156_Arg157insPheProArgSerGly
XM_005261069.3:c.503_504insCTTTCCTCGAAGTGG XP_005261126.1:p.Gly168_Arg169insPheProArgSerGly
XM_011529766.1:c.503_504insCTTTCCTCGAAGTGG XP_011528068.1:p.Gly168_Arg169insPheProArgSerGly
XM_011529767.1:c.464_465insCTTTCCTCGAAGTGG XP_011528069.1:p.Gly155_Arg156insPheProArgSerGly
XM_011529768.1:c.464_465insCTTTCCTCGAAGTGG XP_011528070.1:p.Gly155_Arg156insPheProArgSerGly
XM_011529770.1:c.503_504insCTTTCCTCGAAGTGG XP_011528072.1:p.Gly168_Arg169insPheProArgSerGly
XR_937576.1:n.682_683insCTTTCCTCGAAGTGG
XM_005261069.4:c.503_504insCTTTCCTCGAAGTGG XP_005261126.1:p.Gly168_Arg169insPheProArgSerGly
XM_011529766.2:c.503_504insCTTTCCTCGAAGTGG XP_011528068.1:p.Gly168_Arg169insPheProArgSerGly
XM_011529767.2:c.464_465insCTTTCCTCGAAGTGG XP_011528069.1:p.Gly155_Arg156insPheProArgSerGly
XM_011529768.2:c.464_465insCTTTCCTCGAAGTGG XP_011528070.1:p.Gly155_Arg156insPheProArgSerGly
XM_011529770.2:c.503_504insCTTTCCTCGAAGTGG XP_011528072.1:p.Gly168_Arg169insPheProArgSerGly
XM_017028487.1:c.350_351insCTTTCCTCGAAGTGG XP_016883976.1:p.Gly117_Arg118insPheProArgSerGly
XR_937576.2:n.729_730insCTTTCCTCGAAGTGG
NM_001001890.3:c.422_423insCTTTCCTCGAAGTGG NP_001001890.1:p.Gly141_Arg142insPheProArgSerGly
NM_001122607.2:c.422_423insCTTTCCTCGAAGTGG NP_001116079.1:p.Gly141_Arg142insPheProArgSerGly
NM_001754.5:c.503_504insCTTTCCTCGAAGTGG MANE Select NP_001745.2:p.Gly168_Arg169insPheProArgSerGly
Search 100 bp 5'
Search 100 bp 3'