Canonical Allele Identifier: CA645607442
Gene: RUNX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.34886909_34886910insCCA , CM000683.2:g.34886909_34886910insCCA GRCh38
NC_000021.8:g.36259206_36259207insCCA , CM000683.1:g.36259206_36259207insCCA GRCh37
NC_000021.7:g.35181076_35181077insCCA NCBI36
NG_011402.2:g.1102802_1102803insTGG , LRG_482:g.1102802_1102803insTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000675419.1:c.284_285insTGG MANE Select ENSP00000501943.1:p.Pro95_Asn96insGly
ENST00000300305.7:c.284_285insTGG ENSP00000300305.3:p.Pro95_Asn96insGly
ENST00000344691.8:c.203_204insTGG ENSP00000340690.4:p.Pro68_Asn69insGly
ENST00000358356.9:c.203_204insTGG ENSP00000351123.5:p.Pro68_Asn69insGly
ENST00000399237.6:c.248_249insTGG ENSP00000382182.2:p.Pro83_Asn84insGly
ENST00000399240.5:c.203_204insTGG ENSP00000382184.1:p.Pro68_Asn69insGly
ENST00000437180.5:c.284_285insTGG ENSP00000409227.1:p.Pro95_Asn96insGly
ENST00000455571.5:c.245_246insTGG ENSP00000388189.1:p.Pro82_Asn83insGly
ENST00000482318.5:c.59-6197_59-6196insTGG ENSP00000477067.1:n.59-6197_59-6196insTGG
NM_001001890.2:c.203_204insTGG NP_001001890.1:p.Pro68_Asn69insGly
NM_001122607.1:c.203_204insTGG NP_001116079.1:p.Pro68_Asn69insGly
NM_001754.4:c.284_285insTGG , LRG_482t1:c.284_285insTGG NP_001745.2:p.Pro95_Asn96insGly
XM_005261068.3:c.248_249insTGG XP_005261125.1:p.Pro83_Asn84insGly
XM_005261069.3:c.284_285insTGG XP_005261126.1:p.Pro95_Asn96insGly
XM_011529766.1:c.284_285insTGG XP_011528068.1:p.Pro95_Asn96insGly
XM_011529767.1:c.245_246insTGG XP_011528069.1:p.Pro82_Asn83insGly
XM_011529768.1:c.245_246insTGG XP_011528070.1:p.Pro82_Asn83insGly
XM_011529770.1:c.284_285insTGG XP_011528072.1:p.Pro95_Asn96insGly
XR_937576.1:n.463_464insTGG
XM_005261069.4:c.284_285insTGG XP_005261126.1:p.Pro95_Asn96insGly
XM_011529766.2:c.284_285insTGG XP_011528068.1:p.Pro95_Asn96insGly
XM_011529767.2:c.245_246insTGG XP_011528069.1:p.Pro82_Asn83insGly
XM_011529768.2:c.245_246insTGG XP_011528070.1:p.Pro82_Asn83insGly
XM_011529770.2:c.284_285insTGG XP_011528072.1:p.Pro95_Asn96insGly
XM_017028487.1:c.131_132insTGG XP_016883976.1:p.Pro44_Asn45insGly
XR_937576.2:n.510_511insTGG
NM_001001890.3:c.203_204insTGG NP_001001890.1:p.Pro68_Asn69insGly
NM_001122607.2:c.203_204insTGG NP_001116079.1:p.Pro68_Asn69insGly
NM_001754.5:c.284_285insTGG MANE Select NP_001745.2:p.Pro95_Asn96insGly