Canonical Allele Identifier: CA2678973954
Gene: RUNX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.45547374_45547380del , CM000668.2:g.45547374_45547380del GRCh38
NC_000006.11:g.45515111_45515117del , CM000668.1:g.45515111_45515117del GRCh37
NC_000006.10:g.45623089_45623095del NCBI36
NG_008020.1:g.224058_224064del
NG_008020.2:g.224058_224064del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646519.1:c.*792_*798del ENSP00000496517.1:n.*792_*798del
ENST00000647337.2:c.*69_*75del MANE Select ENSP00000495497.1:n.*69_*75del
ENST00000359524.7:c.*69_*75del ENSP00000352514.5:n.*69_*75del
ENST00000371432.7:c.*69_*75del ENSP00000360486.4:n.*69_*75del
ENST00000371436.10:c.1569_1575del ENSP00000360491.6:n.1569_1575del
ENST00000371438.5:c.*69_*75del ENSP00000360493.1:n.*69_*75del
ENST00000478660.6:c.*178+33721_*178+33727del ENSP00000460188.1:n.*178+33721_*178+33727del
ENST00000576263.5:c.1021+34967_1021+34973del ENSP00000458178.1:n.1021+34967_1021+34973del
NM_001015051.3:c.*69_*75del NP_001015051.3:n.*69_*75del
NM_001024630.3:c.*69_*75del NP_001019801.3:n.*69_*75del
NM_001278478.1:c.1527_1533del NP_001265407.1:n.1527_1533del
XM_006715232.1:c.*69_*75del XP_006715295.1:n.*69_*75del
XM_011514960.1:c.1225+34967_1225+34973del XP_011513262.1:n.1225+34967_1225+34973del
XM_011514961.1:c.*69_*75del XP_011513263.1:n.*69_*75del
XM_011514962.1:c.*69_*75del XP_011513264.1:n.*69_*75del
XM_011514963.1:c.1051+34967_1051+34973del XP_011513265.1:n.1051+34967_1051+34973del
XM_011514964.1:c.1435+404_1435+410del XP_011513266.1:n.1435+404_1435+410del
XM_011514966.1:c.553+34967_553+34973del XP_011513268.1:n.553+34967_553+34973del
NM_001024630.4:c.*69_*75del MANE Select NP_001019801.3:n.*69_*75del
NM_001278478.2:c.*69_*75del NP_001265407.1:n.*69_*75del
NM_001369405.1:c.*69_*75del NP_001356334.1:n.*69_*75del
NM_001015051.4:c.*69_*75del NP_001015051.3:n.*69_*75del