Canonical Allele Identifier: CA320642597

Gene: RUNX1

Linked Data

• dbSNP Id: rs985566660
• MyVariant Identifiers: chr21:g.36259140C>T (hg19) ; chr21:g.34886843C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34886843C>T , CM000683.2:g.34886843C>T	GRCh38
NC_000021.8:g.36259140C>T , CM000683.1:g.36259140C>T	GRCh37
NC_000021.7:g.35181010C>T	NCBI36
NG_011402.2:g.1102869G>A , LRG_482:g.1102869G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000675419.1:c.351G>A MANE Select	ENSP00000501943.1:p.Lys117=
ENST00000300305.7:c.351G>A	ENSP00000300305.3:p.Lys117=
ENST00000344691.8:c.270G>A	ENSP00000340690.4:p.Lys90=
ENST00000358356.9:c.270G>A	ENSP00000351123.5:p.Lys90=
ENST00000399237.6:c.315G>A	ENSP00000382182.2:p.Lys105=
ENST00000399240.5:c.270G>A	ENSP00000382184.1:p.Lys90=
ENST00000437180.5:c.351G>A	ENSP00000409227.1:p.Lys117=
ENST00000455571.5:c.312G>A	ENSP00000388189.1:p.Lys104=
ENST00000482318.5:c.59-6130G>A	ENSP00000477067.1:n.59-6130G>A
NM_001001890.2:c.270G>A	NP_001001890.1:p.Lys90=
NM_001122607.1:c.270G>A	NP_001116079.1:p.Lys90=
NM_001754.4:c.351G>A , LRG_482t1:c.351G>A	NP_001745.2:p.Lys117=
XM_005261068.3:c.315G>A	XP_005261125.1:p.Lys105=
XM_005261069.3:c.351G>A	XP_005261126.1:p.Lys117=
XM_011529766.1:c.351G>A	XP_011528068.1:p.Lys117=
XM_011529767.1:c.312G>A	XP_011528069.1:p.Lys104=
XM_011529768.1:c.312G>A	XP_011528070.1:p.Lys104=
XM_011529770.1:c.351G>A	XP_011528072.1:p.Lys117=
XR_937576.1:n.530G>A
XM_005261069.4:c.351G>A	XP_005261126.1:p.Lys117=
XM_011529766.2:c.351G>A	XP_011528068.1:p.Lys117=
XM_011529767.2:c.312G>A	XP_011528069.1:p.Lys104=
XM_011529768.2:c.312G>A	XP_011528070.1:p.Lys104=
XM_011529770.2:c.351G>A	XP_011528072.1:p.Lys117=
XM_017028487.1:c.198G>A	XP_016883976.1:p.Lys66=
XR_937576.2:n.577G>A
NM_001001890.3:c.270G>A	NP_001001890.1:p.Lys90=
NM_001122607.2:c.270G>A	NP_001116079.1:p.Lys90=
NM_001754.5:c.351G>A MANE Select	NP_001745.2:p.Lys117=