Canonical Allele Identifier: CA410202656
Gene: RUNX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr21:g.36252945G>T (hg19) chr21:g.34880648G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880648G>T , CM000683.2:g.34880648G>T GRCh38
NC_000021.8:g.36252945G>T , CM000683.1:g.36252945G>T GRCh37
NC_000021.7:g.35174815G>T NCBI36
NG_011402.2:g.1109064C>A , LRG_482:g.1109064C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.417C>A MANE Select ENSP00000501943.1:p.Asn139Lys
ENST00000300305.7:c.417C>A ENSP00000300305.3:p.Asn139Lys
ENST00000344691.8:c.336C>A ENSP00000340690.4:p.Asn112Lys
ENST00000358356.9:c.336C>A ENSP00000351123.5:p.Asn112Lys
ENST00000399237.6:c.381C>A ENSP00000382182.2:p.Asn127Lys
ENST00000399240.5:c.336C>A ENSP00000382184.1:p.Asn112Lys
ENST00000437180.5:c.417C>A ENSP00000409227.1:p.Asn139Lys
ENST00000455571.5:c.378C>A ENSP00000388189.1:p.Asn126Lys
ENST00000482318.5:c.*7C>A ENSP00000477067.1:n.*7C>A
NM_001001890.2:c.336C>A NP_001001890.1:p.Asn112Lys
NM_001122607.1:c.336C>A NP_001116079.1:p.Asn112Lys
NM_001754.4:c.417C>A , LRG_482t1:c.417C>A NP_001745.2:p.Asn139Lys
XM_005261068.3:c.381C>A XP_005261125.1:p.Asn127Lys
XM_005261069.3:c.417C>A XP_005261126.1:p.Asn139Lys
XM_011529766.1:c.417C>A XP_011528068.1:p.Asn139Lys
XM_011529767.1:c.378C>A XP_011528069.1:p.Asn126Lys
XM_011529768.1:c.378C>A XP_011528070.1:p.Asn126Lys
XM_011529770.1:c.417C>A XP_011528072.1:p.Asn139Lys
XR_937576.1:n.596C>A
XM_005261069.4:c.417C>A XP_005261126.1:p.Asn139Lys
XM_011529766.2:c.417C>A XP_011528068.1:p.Asn139Lys
XM_011529767.2:c.378C>A XP_011528069.1:p.Asn126Lys
XM_011529768.2:c.378C>A XP_011528070.1:p.Asn126Lys
XM_011529770.2:c.417C>A XP_011528072.1:p.Asn139Lys
XM_017028487.1:c.264C>A XP_016883976.1:p.Asn88Lys
XR_937576.2:n.643C>A
NM_001001890.3:c.336C>A NP_001001890.1:p.Asn112Lys
NM_001122607.2:c.336C>A NP_001116079.1:p.Asn112Lys
NM_001754.5:c.417C>A MANE Select NP_001745.2:p.Asn139Lys
Search 100 bp 5'
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