Canonical Allele Identifier: CA10014629
Community Standard Title: NM_001754.5(RUNX1):c.97G>A (p.Asp33Asn)
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34892925C>T , CM000683.2:g.34892925C>T GRCh38
NC_000021.8:g.36265222C>T , CM000683.1:g.36265222C>T GRCh37
NC_000021.7:g.35187092C>T NCBI36
NG_011402.2:g.1096787G>A , LRG_482:g.1096787G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001754.5:c.97G>A MANE Select NP_001745.2:p.Asp33Asn
ENST00000675419.1:c.97G>A MANE Select ENSP00000501943.1:p.Asp33Asn
NM_001754.4:c.97G>A , LRG_482t1:c.97G>A NP_001745.2:p.Asp33Asn
ENST00000300305.7:c.97G>A ENSP00000300305.3:p.Asp33Asn
ENST00000416754.1:c.97G>A
ENST00000437180.5:c.97G>A ENSP00000409227.1:p.Asp33Asn
ENST00000455571.5:c.59-5829G>A ENSP00000388189.1:n.59-5829G>A
ENST00000475045.6:c.97G>A ENSP00000477072.1:p.Asp33Asn
ENST00000482318.5:c.59-12212G>A ENSP00000477067.1:n.59-12212G>A
XM_005261069.3:c.97G>A XP_005261126.1:p.Asp33Asn
XM_005261069.4:c.97G>A XP_005261126.1:p.Asp33Asn
XM_011529766.1:c.97G>A XP_011528068.1:p.Asp33Asn
XM_011529766.2:c.97G>A XP_011528068.1:p.Asp33Asn
XM_011529767.1:c.59-5829G>A XP_011528069.1:n.59-5829G>A
XM_011529767.2:c.59-5829G>A XP_011528069.1:n.59-5829G>A
XM_011529768.1:c.59-5829G>A XP_011528070.1:n.59-5829G>A
XM_011529768.2:c.59-5829G>A XP_011528070.1:n.59-5829G>A
XM_011529770.1:c.97G>A XP_011528072.1:p.Asp33Asn
XM_011529770.2:c.97G>A XP_011528072.1:p.Asp33Asn
XR_937576.1:n.276G>A
XR_937576.2:n.323G>A