Canonical Allele Identifier: CA891842373
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880647_34880709dup , CM000683.2:g.34880647_34880709dup GRCh38
NC_000021.8:g.36252944_36253006dup , CM000683.1:g.36252944_36253006dup GRCh37
NC_000021.7:g.35174814_35174876dup NCBI36
NG_011402.2:g.1109003_1109065dup , LRG_482:g.1109003_1109065dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.356_418dup MANE Select ENSP00000501943.1:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspG...
ENST00000300305.7:c.356_418dup ENSP00000300305.3:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspG...
ENST00000344691.8:c.275_337dup ENSP00000340690.4:p.Asn112_Tyr113insLeuAlaLeuGlyAspValProAspG...
ENST00000358356.9:c.275_337dup ENSP00000351123.5:p.Asn112_Tyr113insLeuAlaLeuGlyAspValProAspG...
ENST00000399237.6:c.320_382dup ENSP00000382182.2:p.Asn127_Tyr128insLeuAlaLeuGlyAspValProAspG...
ENST00000399240.5:c.275_337dup ENSP00000382184.1:p.Asn112_Tyr113insLeuAlaLeuGlyAspValProAspG...
ENST00000437180.5:c.356_418dup ENSP00000409227.1:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspG...
ENST00000455571.5:c.317_379dup ENSP00000388189.1:p.Asn126_Tyr127insLeuAlaLeuGlyAspValProAspG...
ENST00000482318.5:c.63_*8dup ENSP00000477067.1:n.63_*8dup
NM_001001890.2:c.275_337dup NP_001001890.1:p.Asn112_Tyr113insLeuAlaLeuGlyAspValProAspGlyT...
NM_001122607.1:c.275_337dup NP_001116079.1:p.Asn112_Tyr113insLeuAlaLeuGlyAspValProAspGlyT...
NM_001754.4:c.356_418dup , LRG_482t1:c.356_418dup NP_001745.2:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspGlyThrL...
XM_005261068.3:c.320_382dup XP_005261125.1:p.Asn127_Tyr128insLeuAlaLeuGlyAspValProAspGlyT...
XM_005261069.3:c.356_418dup XP_005261126.1:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspGlyT...
XM_011529766.1:c.356_418dup XP_011528068.1:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspGlyT...
XM_011529767.1:c.317_379dup XP_011528069.1:p.Asn126_Tyr127insLeuAlaLeuGlyAspValProAspGlyT...
XM_011529768.1:c.317_379dup XP_011528070.1:p.Asn126_Tyr127insLeuAlaLeuGlyAspValProAspGlyT...
XM_011529770.1:c.356_418dup XP_011528072.1:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspGlyT...
XR_937576.1:n.535_597dup
XM_005261069.4:c.356_418dup XP_005261126.1:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspGlyT...
XM_011529766.2:c.356_418dup XP_011528068.1:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspGlyT...
XM_011529767.2:c.317_379dup XP_011528069.1:p.Asn126_Tyr127insLeuAlaLeuGlyAspValProAspGlyT...
XM_011529768.2:c.317_379dup XP_011528070.1:p.Asn126_Tyr127insLeuAlaLeuGlyAspValProAspGlyT...
XM_011529770.2:c.356_418dup XP_011528072.1:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspGlyT...
XM_017028487.1:c.203_265dup XP_016883976.1:p.Asn88_Tyr89insLeuAlaLeuGlyAspValProAspGlyThr...
XR_937576.2:n.582_644dup
NM_001001890.3:c.275_337dup NP_001001890.1:p.Asn112_Tyr113insLeuAlaLeuGlyAspValProAspGlyT...
NM_001122607.2:c.275_337dup NP_001116079.1:p.Asn112_Tyr113insLeuAlaLeuGlyAspValProAspGlyT...
NM_001754.5:c.356_418dup MANE Select NP_001745.2:p.Asn139_Tyr140insLeuAlaLeuGlyAspValProAspGlyThrL...