Canonical Allele Identifier: CA645607364
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM5031006 COSM5031007
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880625_34880626delinsAAAAGGCA , CM000683.2:g.34880625_34880626delinsAAAAGGCA GRCh38
NC_000021.8:g.36252922_36252923delinsAAAAGGCA , CM000683.1:g.36252922_36252923delinsAAAAGGCA GRCh37
NC_000021.7:g.35174792_35174793delinsAAAAGGCA NCBI36
NG_011402.2:g.1109086_1109087delinsTGCCTTTT , LRG_482:g.1109086_1109087delinsTGCCTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.439_440delinsTGCCTTTT MANE Select ENSP00000501943.1:p.Ala147delinsCysLeuPhe
ENST00000300305.7:c.439_440delinsTGCCTTTT ENSP00000300305.3:p.Ala147delinsCysLeuPhe
ENST00000344691.8:c.358_359delinsTGCCTTTT ENSP00000340690.4:p.Ala120delinsCysLeuPhe
ENST00000358356.9:c.358_359delinsTGCCTTTT ENSP00000351123.5:p.Ala120delinsCysLeuPhe
ENST00000399237.6:c.403_404delinsTGCCTTTT ENSP00000382182.2:p.Ala135delinsCysLeuPhe
ENST00000399240.5:c.358_359delinsTGCCTTTT ENSP00000382184.1:p.Ala120delinsCysLeuPhe
ENST00000437180.5:c.439_440delinsTGCCTTTT ENSP00000409227.1:p.Ala147delinsCysLeuPhe
ENST00000455571.5:c.400_401delinsTGCCTTTT ENSP00000388189.1:p.Ala134delinsCysLeuPhe
ENST00000482318.5:c.*29_*30delinsTGCCTTTT ENSP00000477067.1:n.*29_*30delinsTGCCTTTT
NM_001001890.2:c.358_359delinsTGCCTTTT NP_001001890.1:p.Ala120delinsCysLeuPhe
NM_001122607.1:c.358_359delinsTGCCTTTT NP_001116079.1:p.Ala120delinsCysLeuPhe
NM_001754.4:c.439_440delinsTGCCTTTT , LRG_482t1:c.439_440delinsTGCCTTTT NP_001745.2:p.Ala147delinsCysLeuPhe
XM_005261068.3:c.403_404delinsTGCCTTTT XP_005261125.1:p.Ala135delinsCysLeuPhe
XM_005261069.3:c.439_440delinsTGCCTTTT XP_005261126.1:p.Ala147delinsCysLeuPhe
XM_011529766.1:c.439_440delinsTGCCTTTT XP_011528068.1:p.Ala147delinsCysLeuPhe
XM_011529767.1:c.400_401delinsTGCCTTTT XP_011528069.1:p.Ala134delinsCysLeuPhe
XM_011529768.1:c.400_401delinsTGCCTTTT XP_011528070.1:p.Ala134delinsCysLeuPhe
XM_011529770.1:c.439_440delinsTGCCTTTT XP_011528072.1:p.Ala147delinsCysLeuPhe
XR_937576.1:n.618_619delinsTGCCTTTT
XM_005261069.4:c.439_440delinsTGCCTTTT XP_005261126.1:p.Ala147delinsCysLeuPhe
XM_011529766.2:c.439_440delinsTGCCTTTT XP_011528068.1:p.Ala147delinsCysLeuPhe
XM_011529767.2:c.400_401delinsTGCCTTTT XP_011528069.1:p.Ala134delinsCysLeuPhe
XM_011529768.2:c.400_401delinsTGCCTTTT XP_011528070.1:p.Ala134delinsCysLeuPhe
XM_011529770.2:c.439_440delinsTGCCTTTT XP_011528072.1:p.Ala147delinsCysLeuPhe
XM_017028487.1:c.286_287delinsTGCCTTTT XP_016883976.1:p.Ala96delinsCysLeuPhe
XR_937576.2:n.665_666delinsTGCCTTTT
NM_001001890.3:c.358_359delinsTGCCTTTT NP_001001890.1:p.Ala120delinsCysLeuPhe
NM_001122607.2:c.358_359delinsTGCCTTTT NP_001116079.1:p.Ala120delinsCysLeuPhe
NM_001754.5:c.439_440delinsTGCCTTTT MANE Select NP_001745.2:p.Ala147delinsCysLeuPhe
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