Canonical Allele Identifier: CA512318855
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886907_34886908insA , CM000683.2:g.34886907_34886908insA GRCh38
NC_000021.8:g.36259204_36259205insA , CM000683.1:g.36259204_36259205insA GRCh37
NC_000021.7:g.35181074_35181075insA NCBI36
NG_011402.2:g.1102804_1102805insT , LRG_482:g.1102804_1102805insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.286_287insT MANE Select ENSP00000501943.1:p.Asn96IlefsTer?
ENST00000300305.7:c.286_287insT ENSP00000300305.3:p.Asn96IlefsTer?
ENST00000344691.8:c.205_206insT ENSP00000340690.4:p.Asn69IlefsTer?
ENST00000358356.9:c.205_206insT ENSP00000351123.5:p.Asn69IlefsTer?
ENST00000399237.6:c.250_251insT ENSP00000382182.2:p.Asn84IlefsTer?
ENST00000399240.5:c.205_206insT ENSP00000382184.1:p.Asn69IlefsTer?
ENST00000437180.5:c.286_287insT ENSP00000409227.1:p.Asn96IlefsTer?
ENST00000455571.5:c.247_248insT ENSP00000388189.1:p.Asn83IlefsTer?
ENST00000482318.5:c.59-6195_59-6194insT ENSP00000477067.1:n.59-6195_59-6194insT
NM_001001890.2:c.205_206insT NP_001001890.1:p.Asn69IlefsTer?
NM_001122607.1:c.205_206insT NP_001116079.1:p.Asn69IlefsTer?
NM_001754.4:c.286_287insT , LRG_482t1:c.286_287insT NP_001745.2:p.Asn96IlefsTer?
XM_005261068.3:c.250_251insT XP_005261125.1:p.Asn84IlefsTer?
XM_005261069.3:c.286_287insT XP_005261126.1:p.Asn96IlefsTer?
XM_011529766.1:c.286_287insT XP_011528068.1:p.Asn96IlefsTer?
XM_011529767.1:c.247_248insT XP_011528069.1:p.Asn83IlefsTer?
XM_011529768.1:c.247_248insT XP_011528070.1:p.Asn83IlefsTer?
XM_011529770.1:c.286_287insT XP_011528072.1:p.Asn96IlefsTer?
XR_937576.1:n.465_466insT
XM_005261069.4:c.286_287insT XP_005261126.1:p.Asn96IlefsTer?
XM_011529766.2:c.286_287insT XP_011528068.1:p.Asn96IlefsTer?
XM_011529767.2:c.247_248insT XP_011528069.1:p.Asn83IlefsTer?
XM_011529768.2:c.247_248insT XP_011528070.1:p.Asn83IlefsTer?
XM_011529770.2:c.286_287insT XP_011528072.1:p.Asn96IlefsTer?
XM_017028487.1:c.133_134insT XP_016883976.1:p.Asn45IlefsTer?
XR_937576.2:n.512_513insT
NM_001001890.3:c.205_206insT NP_001001890.1:p.Asn69IlefsTer?
NM_001122607.2:c.205_206insT NP_001116079.1:p.Asn69IlefsTer?
NM_001754.5:c.286_287insT MANE Select NP_001745.2:p.Asn96IlefsTer?