Canonical Allele Identifier: CA645607448
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886936_34886937insAC , CM000683.2:g.34886936_34886937insAC GRCh38
NC_000021.8:g.36259233_36259234insAC , CM000683.1:g.36259233_36259234insAC GRCh37
NC_000021.7:g.35181103_35181104insAC NCBI36
NG_011402.2:g.1102776_1102777insTG , LRG_482:g.1102776_1102777insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.258_259insTG MANE Select ENSP00000501943.1:p.Gly87TrpfsTer?
ENST00000300305.7:c.258_259insTG ENSP00000300305.3:p.Gly87TrpfsTer?
ENST00000344691.8:c.177_178insTG ENSP00000340690.4:p.Gly60TrpfsTer?
ENST00000358356.9:c.177_178insTG ENSP00000351123.5:p.Gly60TrpfsTer?
ENST00000399237.6:c.222_223insTG ENSP00000382182.2:p.Gly75TrpfsTer?
ENST00000399240.5:c.177_178insTG ENSP00000382184.1:p.Gly60TrpfsTer?
ENST00000437180.5:c.258_259insTG ENSP00000409227.1:p.Gly87TrpfsTer?
ENST00000455571.5:c.219_220insTG ENSP00000388189.1:p.Gly74TrpfsTer?
ENST00000482318.5:c.59-6223_59-6222insTG ENSP00000477067.1:n.59-6223_59-6222insTG
NM_001001890.2:c.177_178insTG NP_001001890.1:p.Gly60TrpfsTer?
NM_001122607.1:c.177_178insTG NP_001116079.1:p.Gly60TrpfsTer?
NM_001754.4:c.258_259insTG , LRG_482t1:c.258_259insTG NP_001745.2:p.Gly87TrpfsTer?
XM_005261068.3:c.222_223insTG XP_005261125.1:p.Gly75TrpfsTer?
XM_005261069.3:c.258_259insTG XP_005261126.1:p.Gly87TrpfsTer?
XM_011529766.1:c.258_259insTG XP_011528068.1:p.Gly87TrpfsTer?
XM_011529767.1:c.219_220insTG XP_011528069.1:p.Gly74TrpfsTer?
XM_011529768.1:c.219_220insTG XP_011528070.1:p.Gly74TrpfsTer?
XM_011529770.1:c.258_259insTG XP_011528072.1:p.Gly87TrpfsTer?
XR_937576.1:n.437_438insTG
XM_005261069.4:c.258_259insTG XP_005261126.1:p.Gly87TrpfsTer?
XM_011529766.2:c.258_259insTG XP_011528068.1:p.Gly87TrpfsTer?
XM_011529767.2:c.219_220insTG XP_011528069.1:p.Gly74TrpfsTer?
XM_011529768.2:c.219_220insTG XP_011528070.1:p.Gly74TrpfsTer?
XM_011529770.2:c.258_259insTG XP_011528072.1:p.Gly87TrpfsTer?
XM_017028487.1:c.105_106insTG XP_016883976.1:p.Gly36TrpfsTer?
XR_937576.2:n.484_485insTG
NM_001001890.3:c.177_178insTG NP_001001890.1:p.Gly60TrpfsTer?
NM_001122607.2:c.177_178insTG NP_001116079.1:p.Gly60TrpfsTer?
NM_001754.5:c.258_259insTG MANE Select NP_001745.2:p.Gly87TrpfsTer?