Canonical Allele Identifier: CA410148642
Community Standard Title: NM_001754.5(RUNX1):c.1007T>G (p.Phe336Cys)
Gene: RUNX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34792571A>C , CM000683.2:g.34792571A>C GRCh38
NC_000021.8:g.36164868A>C , CM000683.1:g.36164868A>C GRCh37
NC_000021.7:g.35086738A>C NCBI36
NG_011402.2:g.1197141T>G , LRG_482:g.1197141T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001754.5:c.1007T>G MANE Select NP_001745.2:p.Phe336Cys
ENST00000675419.1:c.1007T>G MANE Select ENSP00000501943.1:p.Phe336Cys
NM_001001890.2:c.926T>G NP_001001890.1:p.Phe309Cys
NM_001001890.3:c.926T>G NP_001001890.1:p.Phe309Cys
NM_001754.4:c.1007T>G , LRG_482t1:c.1007T>G NP_001745.2:p.Phe336Cys
ENST00000300305.7:c.1007T>G ENSP00000300305.3:p.Phe336Cys
ENST00000344691.8:c.926T>G ENSP00000340690.4:p.Phe309Cys
ENST00000399240.5:c.734T>G ENSP00000382184.1:p.Phe245Cys
ENST00000437180.5:c.1007T>G ENSP00000409227.1:p.Phe336Cys
ENST00000482318.5:c.*597T>G ENSP00000477067.1:n.*597T>G
XM_005261068.3:c.971T>G XP_005261125.1:p.Phe324Cys
XM_005261069.3:c.815T>G XP_005261126.1:p.Phe272Cys
XM_005261069.4:c.815T>G XP_005261126.1:p.Phe272Cys
XM_011529766.1:c.1007T>G XP_011528068.1:p.Phe336Cys
XM_011529766.2:c.1007T>G XP_011528068.1:p.Phe336Cys
XM_011529767.1:c.968T>G XP_011528069.1:p.Phe323Cys
XM_011529767.2:c.968T>G XP_011528069.1:p.Phe323Cys
XM_011529768.1:c.776T>G XP_011528070.1:p.Phe259Cys
XM_011529768.2:c.776T>G XP_011528070.1:p.Phe259Cys
XM_017028487.1:c.854T>G XP_016883976.1:p.Phe285Cys
XR_937576.1:n.4611T>G
XR_937576.2:n.4658T>G
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