Canonical Allele Identifier: CA916086495
Gene: RUNX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34887030_34887031insT , CM000683.2:g.34887030_34887031insT GRCh38
NC_000021.8:g.36259327_36259328insT , CM000683.1:g.36259327_36259328insT GRCh37
NC_000021.7:g.35181197_35181198insT NCBI36
NG_011402.2:g.1102681_1102682insA , LRG_482:g.1102681_1102682insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.163_164insA MANE Select ENSP00000501943.1:p.Ala55AspfsTer?
ENST00000300305.7:c.163_164insA ENSP00000300305.3:p.Ala55AspfsTer?
ENST00000344691.8:c.82_83insA ENSP00000340690.4:p.Ala28AspfsTer?
ENST00000358356.9:c.82_83insA ENSP00000351123.5:p.Ala28AspfsTer?
ENST00000399237.6:c.127_128insA ENSP00000382182.2:p.Ala43AspfsTer?
ENST00000399240.5:c.82_83insA ENSP00000382184.1:p.Ala28AspfsTer?
ENST00000437180.5:c.163_164insA ENSP00000409227.1:p.Ala55AspfsTer?
ENST00000455571.5:c.124_125insA ENSP00000388189.1:p.Ala42AspfsTer?
ENST00000482318.5:c.59-6318_59-6317insA ENSP00000477067.1:n.59-6318_59-6317insA
NM_001001890.2:c.82_83insA NP_001001890.1:p.Ala28AspfsTer?
NM_001122607.1:c.82_83insA NP_001116079.1:p.Ala28AspfsTer?
NM_001754.4:c.163_164insA , LRG_482t1:c.163_164insA NP_001745.2:p.Ala55AspfsTer?
XM_005261068.3:c.127_128insA XP_005261125.1:p.Ala43AspfsTer?
XM_005261069.3:c.163_164insA XP_005261126.1:p.Ala55AspfsTer?
XM_011529766.1:c.163_164insA XP_011528068.1:p.Ala55AspfsTer?
XM_011529767.1:c.124_125insA XP_011528069.1:p.Ala42AspfsTer?
XM_011529768.1:c.124_125insA XP_011528070.1:p.Ala42AspfsTer?
XM_011529770.1:c.163_164insA XP_011528072.1:p.Ala55AspfsTer?
XR_937576.1:n.342_343insA
XM_005261069.4:c.163_164insA XP_005261126.1:p.Ala55AspfsTer?
XM_011529766.2:c.163_164insA XP_011528068.1:p.Ala55AspfsTer?
XM_011529767.2:c.124_125insA XP_011528069.1:p.Ala42AspfsTer?
XM_011529768.2:c.124_125insA XP_011528070.1:p.Ala42AspfsTer?
XM_011529770.2:c.163_164insA XP_011528072.1:p.Ala55AspfsTer?
XM_017028487.1:c.10_11insA XP_016883976.1:p.Ala4AspfsTer?
XR_937576.2:n.389_390insA
NM_001001890.3:c.82_83insA NP_001001890.1:p.Ala28AspfsTer?
NM_001122607.2:c.82_83insA NP_001116079.1:p.Ala28AspfsTer?
NM_001754.5:c.163_164insA MANE Select NP_001745.2:p.Ala55AspfsTer?