Canonical Allele Identifier: CA2577483764
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886909_34886913dup , CM000683.2:g.34886909_34886913dup GRCh38
NC_000021.8:g.36259206_36259210dup , CM000683.1:g.36259206_36259210dup GRCh37
NC_000021.7:g.35181076_35181080dup NCBI36
NG_011402.2:g.1102799_1102803dup , LRG_482:g.1102799_1102803dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.281_285dup MANE Select ENSP00000501943.1:p.Asn96AlafsTer28
ENST00000300305.7:c.281_285dup ENSP00000300305.3:p.Asn96AlafsTer28
ENST00000344691.8:c.200_204dup ENSP00000340690.4:p.Asn69AlafsTer28
ENST00000358356.9:c.200_204dup ENSP00000351123.5:p.Asn69AlafsTer28
ENST00000399237.6:c.245_249dup ENSP00000382182.2:p.Asn84AlafsTer28
ENST00000399240.5:c.200_204dup ENSP00000382184.1:p.Asn69AlafsTer28
ENST00000437180.5:c.281_285dup ENSP00000409227.1:p.Asn96AlafsTer28
ENST00000455571.5:c.242_246dup ENSP00000388189.1:p.Asn83AlafsTer28
ENST00000482318.5:c.59-6200_59-6196dup ENSP00000477067.1:n.59-6200_59-6196dup
NM_001001890.2:c.200_204dup NP_001001890.1:p.Asn69AlafsTer28
NM_001122607.1:c.200_204dup NP_001116079.1:p.Asn69AlafsTer28
NM_001754.4:c.281_285dup , LRG_482t1:c.281_285dup NP_001745.2:p.Asn96AlafsTer28
XM_005261068.3:c.245_249dup XP_005261125.1:p.Asn84AlafsTer28
XM_005261069.3:c.281_285dup XP_005261126.1:p.Asn96AlafsTer28
XM_011529766.1:c.281_285dup XP_011528068.1:p.Asn96AlafsTer28
XM_011529767.1:c.242_246dup XP_011528069.1:p.Asn83AlafsTer28
XM_011529768.1:c.242_246dup XP_011528070.1:p.Asn83AlafsTer28
XM_011529770.1:c.281_285dup XP_011528072.1:p.Asn96AlafsTer28
XR_937576.1:n.460_464dup
XM_005261069.4:c.281_285dup XP_005261126.1:p.Asn96AlafsTer28
XM_011529766.2:c.281_285dup XP_011528068.1:p.Asn96AlafsTer28
XM_011529767.2:c.242_246dup XP_011528069.1:p.Asn83AlafsTer28
XM_011529768.2:c.242_246dup XP_011528070.1:p.Asn83AlafsTer28
XM_011529770.2:c.281_285dup XP_011528072.1:p.Asn96AlafsTer28
XM_017028487.1:c.128_132dup XP_016883976.1:p.Asn45AlafsTer28
XR_937576.2:n.507_511dup
NM_001001890.3:c.200_204dup NP_001001890.1:p.Asn69AlafsTer28
NM_001122607.2:c.200_204dup NP_001116079.1:p.Asn69AlafsTer28
NM_001754.5:c.281_285dup MANE Select NP_001745.2:p.Asn96AlafsTer28