Canonical Allele Identifier: CA14906453

Gene: RUNX1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34815749C>T , CM000683.2:g.34815749C>T	GRCh38
NC_000021.8:g.36188046C>T , CM000683.1:g.36188046C>T	GRCh37
NC_000021.7:g.35109916C>T	NCBI36
NG_011402.2:g.1173963G>A , LRG_482:g.1173963G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675419.1:c.806-16287G>A MANE Select	ENSP00000501943.1:n.806-16287G>A
ENST00000300305.7:c.806-16287G>A	ENSP00000300305.3:n.806-16287G>A
ENST00000344691.8:c.725-16287G>A	ENSP00000340690.4:n.725-16287G>A
ENST00000399240.5:c.533-16287G>A	ENSP00000382184.1:n.533-16287G>A
ENST00000437180.5:c.806-16287G>A	ENSP00000409227.1:n.806-16287G>A
ENST00000482318.5:c.*396-16287G>A	ENSP00000477067.1:n.*396-16287G>A
NM_001001890.2:c.725-16287G>A	NP_001001890.1:n.725-16287G>A
NM_001754.4:c.806-16287G>A , LRG_482t1:c.806-16287G>A	NP_001745.2:n.806-16287G>A
XM_005261068.3:c.770-16287G>A	XP_005261125.1:n.770-16287G>A
XM_005261069.3:c.614-16287G>A	XP_005261126.1:n.614-16287G>A
XM_011529766.1:c.806-16287G>A	XP_011528068.1:n.806-16287G>A
XM_011529767.1:c.767-16287G>A	XP_011528069.1:n.767-16287G>A
XM_011529768.1:c.575-16287G>A	XP_011528070.1:n.575-16287G>A
XR_937576.1:n.985-16287G>A
XM_005261069.4:c.614-16287G>A	XP_005261126.1:n.614-16287G>A
XM_011529766.2:c.806-16287G>A	XP_011528068.1:n.806-16287G>A
XM_011529767.2:c.767-16287G>A	XP_011528069.1:n.767-16287G>A
XM_011529768.2:c.575-16287G>A	XP_011528070.1:n.575-16287G>A
XM_017028487.1:c.653-16287G>A	XP_016883976.1:n.653-16287G>A
XR_937576.2:n.1032-16287G>A
NM_001001890.3:c.725-16287G>A	NP_001001890.1:n.725-16287G>A
NM_001754.5:c.806-16287G>A MANE Select	NP_001745.2:n.806-16287G>A