Canonical Allele Identifier: CA410206653
Gene: RUNX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34834413G>A , CM000683.2:g.34834413G>A GRCh38
NC_000021.8:g.36206710G>A , CM000683.1:g.36206710G>A GRCh37
NC_000021.7:g.35128580G>A NCBI36
NG_011402.2:g.1155299C>T , LRG_482:g.1155299C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.802C>T MANE Select ENSP00000501943.1:p.Gln268Ter
ENST00000300305.7:c.802C>T ENSP00000300305.3:p.Gln268Ter
ENST00000344691.8:c.721C>T ENSP00000340690.4:p.Gln241Ter
ENST00000358356.9:c.721C>T ENSP00000351123.5:p.Gln241Ter
ENST00000399237.6:c.766C>T ENSP00000382182.2:p.Gln256Ter
ENST00000399240.5:c.532+25061C>T ENSP00000382184.1:n.532+25061C>T
ENST00000437180.5:c.802C>T ENSP00000409227.1:p.Gln268Ter
ENST00000469087.1:n.338C>T
ENST00000482318.5:c.*392C>T ENSP00000477067.1:n.*392C>T
NM_001001890.2:c.721C>T NP_001001890.1:p.Gln241Ter
NM_001122607.1:c.721C>T NP_001116079.1:p.Gln241Ter
NM_001754.4:c.802C>T , LRG_482t1:c.802C>T NP_001745.2:p.Gln268Ter
XM_005261068.3:c.766C>T XP_005261125.1:p.Gln256Ter
XM_005261069.3:c.613+25061C>T XP_005261126.1:n.613+25061C>T
XM_011529766.1:c.802C>T XP_011528068.1:p.Gln268Ter
XM_011529767.1:c.763C>T XP_011528069.1:p.Gln255Ter
XM_011529768.1:c.574+25061C>T XP_011528070.1:n.574+25061C>T
XM_011529770.1:c.802C>T XP_011528072.1:p.Gln268Ter
XR_937576.1:n.981C>T
XM_005261069.4:c.613+25061C>T XP_005261126.1:n.613+25061C>T
XM_011529766.2:c.802C>T XP_011528068.1:p.Gln268Ter
XM_011529767.2:c.763C>T XP_011528069.1:p.Gln255Ter
XM_011529768.2:c.574+25061C>T XP_011528070.1:n.574+25061C>T
XM_011529770.2:c.802C>T XP_011528072.1:p.Gln268Ter
XM_017028487.1:c.649C>T XP_016883976.1:p.Gln217Ter
XR_937576.2:n.1028C>T
NM_001001890.3:c.721C>T NP_001001890.1:p.Gln241Ter
NM_001122607.2:c.721C>T NP_001116079.1:p.Gln241Ter
NM_001754.5:c.802C>T MANE Select NP_001745.2:p.Gln268Ter
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