Canonical Allele Identifier: CA410203824

Gene: RUNX1

Linked Data

• MyVariant Identifiers: chr21:g.36259251C>G (hg19) ; chr21:g.34886954C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886954C>G , CM000683.2:g.34886954C>G	GRCh38
NC_000021.8:g.36259251C>G , CM000683.1:g.36259251C>G	GRCh37
NC_000021.7:g.35181121C>G	NCBI36
NG_011402.2:g.1102758G>C , LRG_482:g.1102758G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.240G>C MANE Select	ENSP00000501943.1:p.Glu80Asp
ENST00000300305.7:c.240G>C	ENSP00000300305.3:p.Glu80Asp
ENST00000344691.8:c.159G>C	ENSP00000340690.4:p.Glu53Asp
ENST00000358356.9:c.159G>C	ENSP00000351123.5:p.Glu53Asp
ENST00000399237.6:c.204G>C	ENSP00000382182.2:p.Glu68Asp
ENST00000399240.5:c.159G>C	ENSP00000382184.1:p.Glu53Asp
ENST00000437180.5:c.240G>C	ENSP00000409227.1:p.Glu80Asp
ENST00000455571.5:c.201G>C	ENSP00000388189.1:p.Glu67Asp
ENST00000482318.5:c.59-6241G>C	ENSP00000477067.1:n.59-6241G>C
NM_001001890.2:c.159G>C	NP_001001890.1:p.Glu53Asp
NM_001122607.1:c.159G>C	NP_001116079.1:p.Glu53Asp
NM_001754.4:c.240G>C , LRG_482t1:c.240G>C	NP_001745.2:p.Glu80Asp
XM_005261068.3:c.204G>C	XP_005261125.1:p.Glu68Asp
XM_005261069.3:c.240G>C	XP_005261126.1:p.Glu80Asp
XM_011529766.1:c.240G>C	XP_011528068.1:p.Glu80Asp
XM_011529767.1:c.201G>C	XP_011528069.1:p.Glu67Asp
XM_011529768.1:c.201G>C	XP_011528070.1:p.Glu67Asp
XM_011529770.1:c.240G>C	XP_011528072.1:p.Glu80Asp
XR_937576.1:n.419G>C
XM_005261069.4:c.240G>C	XP_005261126.1:p.Glu80Asp
XM_011529766.2:c.240G>C	XP_011528068.1:p.Glu80Asp
XM_011529767.2:c.201G>C	XP_011528069.1:p.Glu67Asp
XM_011529768.2:c.201G>C	XP_011528070.1:p.Glu67Asp
XM_011529770.2:c.240G>C	XP_011528072.1:p.Glu80Asp
XM_017028487.1:c.87G>C	XP_016883976.1:p.Glu29Asp
XR_937576.2:n.466G>C
NM_001001890.3:c.159G>C	NP_001001890.1:p.Glu53Asp
NM_001122607.2:c.159G>C	NP_001116079.1:p.Glu53Asp
NM_001754.5:c.240G>C MANE Select	NP_001745.2:p.Glu80Asp