Canonical Allele Identifier: CA645607343
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM158613

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880573_34880574insGCTAG , CM000683.2:g.34880573_34880574insGCTAG GRCh38
NC_000021.8:g.36252870_36252871insGCTAG , CM000683.1:g.36252870_36252871insGCTAG GRCh37
NC_000021.7:g.35174740_35174741insGCTAG NCBI36
NG_011402.2:g.1109139_1109140insTAGCC , LRG_482:g.1109139_1109140insTAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.492_493insTAGCC MANE Select ENSP00000501943.1:p.Gly165Ter
ENST00000300305.7:c.492_493insTAGCC ENSP00000300305.3:p.Gly165Ter
ENST00000344691.8:c.411_412insTAGCC ENSP00000340690.4:p.Gly138Ter
ENST00000358356.9:c.411_412insTAGCC ENSP00000351123.5:p.Gly138Ter
ENST00000399237.6:c.456_457insTAGCC ENSP00000382182.2:p.Gly153Ter
ENST00000399240.5:c.411_412insTAGCC ENSP00000382184.1:p.Gly138Ter
ENST00000437180.5:c.492_493insTAGCC ENSP00000409227.1:p.Gly165Ter
ENST00000482318.5:c.*82_*83insTAGCC ENSP00000477067.1:n.*82_*83insTAGCC
NM_001001890.2:c.411_412insTAGCC NP_001001890.1:p.Gly138Ter
NM_001122607.1:c.411_412insTAGCC NP_001116079.1:p.Gly138Ter
NM_001754.4:c.492_493insTAGCC , LRG_482t1:c.492_493insTAGCC NP_001745.2:p.Gly165Ter
XM_005261068.3:c.456_457insTAGCC XP_005261125.1:p.Gly153Ter
XM_005261069.3:c.492_493insTAGCC XP_005261126.1:p.Gly165Ter
XM_011529766.1:c.492_493insTAGCC XP_011528068.1:p.Gly165Ter
XM_011529767.1:c.453_454insTAGCC XP_011528069.1:p.Gly152Ter
XM_011529768.1:c.453_454insTAGCC XP_011528070.1:p.Gly152Ter
XM_011529770.1:c.492_493insTAGCC XP_011528072.1:p.Gly165Ter
XR_937576.1:n.671_672insTAGCC
XM_005261069.4:c.492_493insTAGCC XP_005261126.1:p.Gly165Ter
XM_011529766.2:c.492_493insTAGCC XP_011528068.1:p.Gly165Ter
XM_011529767.2:c.453_454insTAGCC XP_011528069.1:p.Gly152Ter
XM_011529768.2:c.453_454insTAGCC XP_011528070.1:p.Gly152Ter
XM_011529770.2:c.492_493insTAGCC XP_011528072.1:p.Gly165Ter
XM_017028487.1:c.339_340insTAGCC XP_016883976.1:p.Gly114Ter
XR_937576.2:n.718_719insTAGCC
NM_001001890.3:c.411_412insTAGCC NP_001001890.1:p.Gly138Ter
NM_001122607.2:c.411_412insTAGCC NP_001116079.1:p.Gly138Ter
NM_001754.5:c.492_493insTAGCC MANE Select NP_001745.2:p.Gly165Ter