Canonical Allele Identifier: CA2387297223
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887034_34887035delinsCG , CM000683.2:g.34887034_34887035delinsCG GRCh38
NC_000021.8:g.36259331_36259332delinsCG , CM000683.1:g.36259331_36259332delinsCG GRCh37
NC_000021.7:g.35181201_35181202delinsCG NCBI36
NG_011402.2:g.1102677_1102678delinsCG , LRG_482:g.1102677_1102678delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.159_160delinsCG MANE Select ENSP00000501943.1:p.Ser53=
ENST00000300305.7:c.159_160delinsCG ENSP00000300305.3:p.Ser53=
ENST00000344691.8:c.78_79delinsCG ENSP00000340690.4:p.Ser26=
ENST00000358356.9:c.78_79delinsCG ENSP00000351123.5:p.Ser26=
ENST00000399237.6:c.123_124delinsCG ENSP00000382182.2:p.Ser41=
ENST00000399240.5:c.78_79delinsCG ENSP00000382184.1:p.Ser26=
ENST00000437180.5:c.159_160delinsCG ENSP00000409227.1:p.Ser53=
ENST00000455571.5:c.120_121delinsCG ENSP00000388189.1:p.Ser40=
ENST00000482318.5:c.59-6322_59-6321delinsCG ENSP00000477067.1:n.59-6322_59-6321delinsCG
NM_001001890.2:c.78_79delinsCG NP_001001890.1:p.Ser26=
NM_001122607.1:c.78_79delinsCG NP_001116079.1:p.Ser26=
NM_001754.4:c.159_160delinsCG , LRG_482t1:c.159_160delinsCG NP_001745.2:p.Ser53=
XM_005261068.3:c.123_124delinsCG XP_005261125.1:p.Ser41=
XM_005261069.3:c.159_160delinsCG XP_005261126.1:p.Ser53=
XM_011529766.1:c.159_160delinsCG XP_011528068.1:p.Ser53=
XM_011529767.1:c.120_121delinsCG XP_011528069.1:p.Ser40=
XM_011529768.1:c.120_121delinsCG XP_011528070.1:p.Ser40=
XM_011529770.1:c.159_160delinsCG XP_011528072.1:p.Ser53=
XR_937576.1:n.338_339delinsCG
XM_005261069.4:c.159_160delinsCG XP_005261126.1:p.Ser53=
XM_011529766.2:c.159_160delinsCG XP_011528068.1:p.Ser53=
XM_011529767.2:c.120_121delinsCG XP_011528069.1:p.Ser40=
XM_011529768.2:c.120_121delinsCG XP_011528070.1:p.Ser40=
XM_011529770.2:c.159_160delinsCG XP_011528072.1:p.Ser53=
XM_017028487.1:c.6_7delinsCG XP_016883976.1:p.Ser2=
XR_937576.2:n.385_386delinsCG
NM_001001890.3:c.78_79delinsCG NP_001001890.1:p.Ser26=
NM_001122607.2:c.78_79delinsCG NP_001116079.1:p.Ser26=
NM_001754.5:c.159_160delinsCG MANE Select NP_001745.2:p.Ser53=