Canonical Allele Identifier: CA10014257
Community Standard Title: NM_001754.5(RUNX1):c.967+8A>T
Gene: RUNX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34799293T>A , CM000683.2:g.34799293T>A GRCh38
NC_000021.8:g.36171590T>A , CM000683.1:g.36171590T>A GRCh37
NC_000021.7:g.35093460T>A NCBI36
NG_011402.2:g.1190419A>T , LRG_482:g.1190419A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001754.5:c.967+8A>T MANE Select NP_001745.2:n.967+8A>T
ENST00000675419.1:c.967+8A>T MANE Select ENSP00000501943.1:n.967+8A>T
NM_001001890.2:c.886+8A>T NP_001001890.1:n.886+8A>T
NM_001001890.3:c.886+8A>T NP_001001890.1:n.886+8A>T
NM_001754.4:c.967+8A>T , LRG_482t1:c.967+8A>T NP_001745.2:n.967+8A>T
ENST00000300305.7:c.967+8A>T ENSP00000300305.3:n.967+8A>T
ENST00000344691.8:c.886+8A>T ENSP00000340690.4:n.886+8A>T
ENST00000399240.5:c.694+8A>T ENSP00000382184.1:n.694+8A>T
ENST00000437180.5:c.967+8A>T ENSP00000409227.1:n.967+8A>T
ENST00000482318.5:c.*557+8A>T ENSP00000477067.1:n.*557+8A>T
XM_005261068.3:c.931+8A>T XP_005261125.1:n.931+8A>T
XM_005261069.3:c.775+8A>T XP_005261126.1:n.775+8A>T
XM_005261069.4:c.775+8A>T XP_005261126.1:n.775+8A>T
XM_011529766.1:c.967+8A>T XP_011528068.1:n.967+8A>T
XM_011529766.2:c.967+8A>T XP_011528068.1:n.967+8A>T
XM_011529767.1:c.928+8A>T XP_011528069.1:n.928+8A>T
XM_011529767.2:c.928+8A>T XP_011528069.1:n.928+8A>T
XM_011529768.1:c.736+8A>T XP_011528070.1:n.736+8A>T
XM_011529768.2:c.736+8A>T XP_011528070.1:n.736+8A>T
XM_017028487.1:c.814+8A>T XP_016883976.1:n.814+8A>T
XR_937576.1:n.1146+8A>T
XR_937576.2:n.1193+8A>T
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