Canonical Allele Identifier: CA645607351
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880593dup , CM000683.2:g.34880593dup GRCh38
NC_000021.8:g.36252890dup , CM000683.1:g.36252890dup GRCh37
NC_000021.7:g.35174760dup NCBI36
NG_011402.2:g.1109121dup , LRG_482:g.1109121dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.474dup MANE Select ENSP00000501943.1:p.Asn159Ter
ENST00000300305.7:c.474dup ENSP00000300305.3:p.Asn159Ter
ENST00000344691.8:c.393dup ENSP00000340690.4:p.Asn132Ter
ENST00000358356.9:c.393dup ENSP00000351123.5:p.Asn132Ter
ENST00000399237.6:c.438dup ENSP00000382182.2:p.Asn147Ter
ENST00000399240.5:c.393dup ENSP00000382184.1:p.Asn132Ter
ENST00000437180.5:c.474dup ENSP00000409227.1:p.Asn159Ter
ENST00000482318.5:c.*64dup ENSP00000477067.1:n.*64dup
NM_001001890.2:c.393dup NP_001001890.1:p.Asn132Ter
NM_001122607.1:c.393dup NP_001116079.1:p.Asn132Ter
NM_001754.4:c.474dup , LRG_482t1:c.474dup NP_001745.2:p.Asn159Ter
XM_005261068.3:c.438dup XP_005261125.1:p.Asn147Ter
XM_005261069.3:c.474dup XP_005261126.1:p.Asn159Ter
XM_011529766.1:c.474dup XP_011528068.1:p.Asn159Ter
XM_011529767.1:c.435dup XP_011528069.1:p.Asn146Ter
XM_011529768.1:c.435dup XP_011528070.1:p.Asn146Ter
XM_011529770.1:c.474dup XP_011528072.1:p.Asn159Ter
XR_937576.1:n.653dup
XM_005261069.4:c.474dup XP_005261126.1:p.Asn159Ter
XM_011529766.2:c.474dup XP_011528068.1:p.Asn159Ter
XM_011529767.2:c.435dup XP_011528069.1:p.Asn146Ter
XM_011529768.2:c.435dup XP_011528070.1:p.Asn146Ter
XM_011529770.2:c.474dup XP_011528072.1:p.Asn159Ter
XM_017028487.1:c.321dup XP_016883976.1:p.Asn108Ter
XR_937576.2:n.700dup
NM_001001890.3:c.393dup NP_001001890.1:p.Asn132Ter
NM_001122607.2:c.393dup NP_001116079.1:p.Asn132Ter
NM_001754.5:c.474dup MANE Select NP_001745.2:p.Asn159Ter