Canonical Allele Identifier: CA645607461
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM4170262
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887016_34887017insCC , CM000683.2:g.34887016_34887017insCC GRCh38
NC_000021.8:g.36259313_36259314insCC , CM000683.1:g.36259313_36259314insCC GRCh37
NC_000021.7:g.35181183_35181184insCC NCBI36
NG_011402.2:g.1102696_1102697insGG , LRG_482:g.1102696_1102697insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.178_179insGG MANE Select ENSP00000501943.1:p.Ala60GlyfsTer13
ENST00000300305.7:c.178_179insGG ENSP00000300305.3:p.Ala60GlyfsTer13
ENST00000344691.8:c.97_98insGG ENSP00000340690.4:p.Ala33GlyfsTer13
ENST00000358356.9:c.97_98insGG ENSP00000351123.5:p.Ala33GlyfsTer13
ENST00000399237.6:c.142_143insGG ENSP00000382182.2:p.Ala48GlyfsTer13
ENST00000399240.5:c.97_98insGG ENSP00000382184.1:p.Ala33GlyfsTer13
ENST00000437180.5:c.178_179insGG ENSP00000409227.1:p.Ala60GlyfsTer13
ENST00000455571.5:c.139_140insGG ENSP00000388189.1:p.Ala47GlyfsTer13
ENST00000482318.5:c.59-6303_59-6302insGG ENSP00000477067.1:n.59-6303_59-6302insGG
NM_001001890.2:c.97_98insGG NP_001001890.1:p.Ala33GlyfsTer13
NM_001122607.1:c.97_98insGG NP_001116079.1:p.Ala33GlyfsTer13
NM_001754.4:c.178_179insGG , LRG_482t1:c.178_179insGG NP_001745.2:p.Ala60GlyfsTer13
XM_005261068.3:c.142_143insGG XP_005261125.1:p.Ala48GlyfsTer13
XM_005261069.3:c.178_179insGG XP_005261126.1:p.Ala60GlyfsTer13
XM_011529766.1:c.178_179insGG XP_011528068.1:p.Ala60GlyfsTer13
XM_011529767.1:c.139_140insGG XP_011528069.1:p.Ala47GlyfsTer13
XM_011529768.1:c.139_140insGG XP_011528070.1:p.Ala47GlyfsTer13
XM_011529770.1:c.178_179insGG XP_011528072.1:p.Ala60GlyfsTer13
XR_937576.1:n.357_358insGG
XM_005261069.4:c.178_179insGG XP_005261126.1:p.Ala60GlyfsTer13
XM_011529766.2:c.178_179insGG XP_011528068.1:p.Ala60GlyfsTer13
XM_011529767.2:c.139_140insGG XP_011528069.1:p.Ala47GlyfsTer13
XM_011529768.2:c.139_140insGG XP_011528070.1:p.Ala47GlyfsTer13
XM_011529770.2:c.178_179insGG XP_011528072.1:p.Ala60GlyfsTer13
XM_017028487.1:c.25_26insGG XP_016883976.1:p.Ala9GlyfsTer13
XR_937576.2:n.404_405insGG
NM_001001890.3:c.97_98insGG NP_001001890.1:p.Ala33GlyfsTer13
NM_001122607.2:c.97_98insGG NP_001116079.1:p.Ala33GlyfsTer13
NM_001754.5:c.178_179insGG MANE Select NP_001745.2:p.Ala60GlyfsTer13
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