Canonical Allele Identifier: CA645607352
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880596_34880597insA , CM000683.2:g.34880596_34880597insA GRCh38
NC_000021.8:g.36252893_36252894insA , CM000683.1:g.36252893_36252894insA GRCh37
NC_000021.7:g.35174763_35174764insA NCBI36
NG_011402.2:g.1109115_1109116insT , LRG_482:g.1109115_1109116insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.468_469insT MANE Select ENSP00000501943.1:p.Arg157Ter
ENST00000300305.7:c.468_469insT ENSP00000300305.3:p.Arg157Ter
ENST00000344691.8:c.387_388insT ENSP00000340690.4:p.Arg130Ter
ENST00000358356.9:c.387_388insT ENSP00000351123.5:p.Arg130Ter
ENST00000399237.6:c.432_433insT ENSP00000382182.2:p.Arg145Ter
ENST00000399240.5:c.387_388insT ENSP00000382184.1:p.Arg130Ter
ENST00000437180.5:c.468_469insT ENSP00000409227.1:p.Arg157Ter
ENST00000482318.5:c.*58_*59insT ENSP00000477067.1:n.*58_*59insT
NM_001001890.2:c.387_388insT NP_001001890.1:p.Arg130Ter
NM_001122607.1:c.387_388insT NP_001116079.1:p.Arg130Ter
NM_001754.4:c.468_469insT , LRG_482t1:c.468_469insT NP_001745.2:p.Arg157Ter
XM_005261068.3:c.432_433insT XP_005261125.1:p.Arg145Ter
XM_005261069.3:c.468_469insT XP_005261126.1:p.Arg157Ter
XM_011529766.1:c.468_469insT XP_011528068.1:p.Arg157Ter
XM_011529767.1:c.429_430insT XP_011528069.1:p.Arg144Ter
XM_011529768.1:c.429_430insT XP_011528070.1:p.Arg144Ter
XM_011529770.1:c.468_469insT XP_011528072.1:p.Arg157Ter
XR_937576.1:n.647_648insT
XM_005261069.4:c.468_469insT XP_005261126.1:p.Arg157Ter
XM_011529766.2:c.468_469insT XP_011528068.1:p.Arg157Ter
XM_011529767.2:c.429_430insT XP_011528069.1:p.Arg144Ter
XM_011529768.2:c.429_430insT XP_011528070.1:p.Arg144Ter
XM_011529770.2:c.468_469insT XP_011528072.1:p.Arg157Ter
XM_017028487.1:c.315_316insT XP_016883976.1:p.Arg106Ter
XR_937576.2:n.694_695insT
NM_001001890.3:c.387_388insT NP_001001890.1:p.Arg130Ter
NM_001122607.2:c.387_388insT NP_001116079.1:p.Arg130Ter
NM_001754.5:c.468_469insT MANE Select NP_001745.2:p.Arg157Ter