Canonical Allele Identifier: CA645607382
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM36058
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880641_34880642insGGAACAGACTTCTT , CM000683.2:g.34880641_34880642insGGAACAGACTTCTT GRCh38
NC_000021.8:g.36252938_36252939insGGAACAGACTTCTT , CM000683.1:g.36252938_36252939insGGAACAGACTTCTT GRCh37
NC_000021.7:g.35174808_35174809insGGAACAGACTTCTT NCBI36
NG_011402.2:g.1109070_1109071insAAGAAGTCTGTTCC , LRG_482:g.1109070_1109071insAAGAAGTCTGTTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.423_424insAAGAAGTCTGTTCC MANE Select ENSP00000501943.1:p.Ala142LysfsTer8
ENST00000300305.7:c.423_424insAAGAAGTCTGTTCC ENSP00000300305.3:p.Ala142LysfsTer8
ENST00000344691.8:c.342_343insAAGAAGTCTGTTCC ENSP00000340690.4:p.Ala115LysfsTer8
ENST00000358356.9:c.342_343insAAGAAGTCTGTTCC ENSP00000351123.5:p.Ala115LysfsTer8
ENST00000399237.6:c.387_388insAAGAAGTCTGTTCC ENSP00000382182.2:p.Ala130LysfsTer8
ENST00000399240.5:c.342_343insAAGAAGTCTGTTCC ENSP00000382184.1:p.Ala115LysfsTer8
ENST00000437180.5:c.423_424insAAGAAGTCTGTTCC ENSP00000409227.1:p.Ala142LysfsTer8
ENST00000455571.5:c.384_385insAAGAAGTCTGTTCC ENSP00000388189.1:p.Ala129LysfsTer8
ENST00000482318.5:c.*13_*14insAAGAAGTCTGTTCC ENSP00000477067.1:n.*13_*14insAAGAAGTCTGTTCC
NM_001001890.2:c.342_343insAAGAAGTCTGTTCC NP_001001890.1:p.Ala115LysfsTer8
NM_001122607.1:c.342_343insAAGAAGTCTGTTCC NP_001116079.1:p.Ala115LysfsTer8
NM_001754.4:c.423_424insAAGAAGTCTGTTCC , LRG_482t1:c.423_424insAAGAAGTCTGTTCC NP_001745.2:p.Ala142LysfsTer8
XM_005261068.3:c.387_388insAAGAAGTCTGTTCC XP_005261125.1:p.Ala130LysfsTer8
XM_005261069.3:c.423_424insAAGAAGTCTGTTCC XP_005261126.1:p.Ala142LysfsTer8
XM_011529766.1:c.423_424insAAGAAGTCTGTTCC XP_011528068.1:p.Ala142LysfsTer8
XM_011529767.1:c.384_385insAAGAAGTCTGTTCC XP_011528069.1:p.Ala129LysfsTer8
XM_011529768.1:c.384_385insAAGAAGTCTGTTCC XP_011528070.1:p.Ala129LysfsTer8
XM_011529770.1:c.423_424insAAGAAGTCTGTTCC XP_011528072.1:p.Ala142LysfsTer8
XR_937576.1:n.602_603insAAGAAGTCTGTTCC
XM_005261069.4:c.423_424insAAGAAGTCTGTTCC XP_005261126.1:p.Ala142LysfsTer8
XM_011529766.2:c.423_424insAAGAAGTCTGTTCC XP_011528068.1:p.Ala142LysfsTer8
XM_011529767.2:c.384_385insAAGAAGTCTGTTCC XP_011528069.1:p.Ala129LysfsTer8
XM_011529768.2:c.384_385insAAGAAGTCTGTTCC XP_011528070.1:p.Ala129LysfsTer8
XM_011529770.2:c.423_424insAAGAAGTCTGTTCC XP_011528072.1:p.Ala142LysfsTer8
XM_017028487.1:c.270_271insAAGAAGTCTGTTCC XP_016883976.1:p.Ala91LysfsTer8
XR_937576.2:n.649_650insAAGAAGTCTGTTCC
NM_001001890.3:c.342_343insAAGAAGTCTGTTCC NP_001001890.1:p.Ala115LysfsTer8
NM_001122607.2:c.342_343insAAGAAGTCTGTTCC NP_001116079.1:p.Ala115LysfsTer8
NM_001754.5:c.423_424insAAGAAGTCTGTTCC MANE Select NP_001745.2:p.Ala142LysfsTer8
Search 100 bp 5'
Search 100 bp 3'