Canonical Allele Identifier: CA2387297154
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886935_34886937delinsCCG , CM000683.2:g.34886935_34886937delinsCCG GRCh38
NC_000021.8:g.36259232_36259234delinsCCG , CM000683.1:g.36259232_36259234delinsCCG GRCh37
NC_000021.7:g.35181102_35181104delinsCCG NCBI36
NG_011402.2:g.1102775_1102777delinsCGG , LRG_482:g.1102775_1102777delinsCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.257_259delinsCGG MANE Select ENSP00000501943.1:p.Pro86=
ENST00000300305.7:c.257_259delinsCGG ENSP00000300305.3:p.Pro86=
ENST00000344691.8:c.176_178delinsCGG ENSP00000340690.4:p.Pro59=
ENST00000358356.9:c.176_178delinsCGG ENSP00000351123.5:p.Pro59=
ENST00000399237.6:c.221_223delinsCGG ENSP00000382182.2:p.Pro74=
ENST00000399240.5:c.176_178delinsCGG ENSP00000382184.1:p.Pro59=
ENST00000437180.5:c.257_259delinsCGG ENSP00000409227.1:p.Pro86=
ENST00000455571.5:c.218_220delinsCGG ENSP00000388189.1:p.Pro73=
ENST00000482318.5:c.59-6224_59-6222delinsCGG ENSP00000477067.1:n.59-6224_59-6222delinsCGG
NM_001001890.2:c.176_178delinsCGG NP_001001890.1:p.Pro59=
NM_001122607.1:c.176_178delinsCGG NP_001116079.1:p.Pro59=
NM_001754.4:c.257_259delinsCGG , LRG_482t1:c.257_259delinsCGG NP_001745.2:p.Pro86=
XM_005261068.3:c.221_223delinsCGG XP_005261125.1:p.Pro74=
XM_005261069.3:c.257_259delinsCGG XP_005261126.1:p.Pro86=
XM_011529766.1:c.257_259delinsCGG XP_011528068.1:p.Pro86=
XM_011529767.1:c.218_220delinsCGG XP_011528069.1:p.Pro73=
XM_011529768.1:c.218_220delinsCGG XP_011528070.1:p.Pro73=
XM_011529770.1:c.257_259delinsCGG XP_011528072.1:p.Pro86=
XR_937576.1:n.436_438delinsCGG
XM_005261069.4:c.257_259delinsCGG XP_005261126.1:p.Pro86=
XM_011529766.2:c.257_259delinsCGG XP_011528068.1:p.Pro86=
XM_011529767.2:c.218_220delinsCGG XP_011528069.1:p.Pro73=
XM_011529768.2:c.218_220delinsCGG XP_011528070.1:p.Pro73=
XM_011529770.2:c.257_259delinsCGG XP_011528072.1:p.Pro86=
XM_017028487.1:c.104_106delinsCGG XP_016883976.1:p.Pro35=
XR_937576.2:n.483_485delinsCGG
NM_001001890.3:c.176_178delinsCGG NP_001001890.1:p.Pro59=
NM_001122607.2:c.176_178delinsCGG NP_001116079.1:p.Pro59=
NM_001754.5:c.257_259delinsCGG MANE Select NP_001745.2:p.Pro86=