Canonical Allele Identifier: CA512318801
Gene: RUNX1 HGNC NCBI

Linked Data

COSMIC: COSM41701
MyVariant Identifiers: chr21:g.36253010del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34880714del , CM000683.2:g.34880714del GRCh38
NC_000021.8:g.36253011del , CM000683.1:g.36253011del GRCh37
NC_000021.7:g.35174881del NCBI36
NG_011402.2:g.1108999del , LRG_482:g.1108999del

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.352del
ENST00000300305.7:c.352del
ENST00000344691.8:c.271del
ENST00000358356.9:c.271del
ENST00000399237.6:c.316del
ENST00000399240.5:c.271del
ENST00000437180.5:c.352del
ENST00000455571.5:c.313del
ENST00000482318.5:c.59del
NM_001001890.2:c.271del
NM_001122607.1:c.271del
NM_001754.4:c.352del , LRG_482t1:c.352del
XM_005261068.3:c.316del
XM_005261069.3:c.352del
XM_011529766.1:c.352del
XM_011529767.1:c.313del
XM_011529768.1:c.313del
XM_011529770.1:c.352del
XR_937576.1:n.531del
XM_005261069.4:c.352del
XM_011529766.2:c.352del
XM_011529767.2:c.313del
XM_011529768.2:c.313del
XM_011529770.2:c.352del
XM_017028487.1:c.199del
XR_937576.2:n.578del
NM_001001890.3:c.271del
NM_001122607.2:c.271del
NM_001754.5:c.352del