Canonical Allele Identifier: CA363957505
Gene: RUNX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.45547304G>T , CM000668.2:g.45547304G>T GRCh38
NC_000006.11:g.45515041G>T , CM000668.1:g.45515041G>T GRCh37
NC_000006.10:g.45623019G>T NCBI36
NG_008020.1:g.223988G>T
NG_008020.2:g.223988G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646519.1:c.*722G>T ENSP00000496517.1:n.*722G>T
ENST00000647337.2:c.1565G>T MANE Select ENSP00000495497.1:p.Ter522Leu
ENST00000359524.7:c.1523G>T ENSP00000352514.5:p.Ter508Leu
ENST00000371432.7:c.1499G>T ENSP00000360486.4:p.Ter500Leu
ENST00000371436.10:c.1499G>T ENSP00000360491.6:p.Ter500Leu
ENST00000371438.5:c.1565G>T ENSP00000360493.1:p.Ter522Leu
ENST00000465038.6:c.1565G>T ENSP00000420707.2:p.Ter522Leu
ENST00000478660.6:c.*178+33651G>T ENSP00000460188.1:n.*178+33651G>T
ENST00000576263.5:c.1021+34897G>T ENSP00000458178.1:n.1021+34897G>T
ENST00000625924.1:c.1457G>T ENSP00000485863.1:p.Ter486Leu
NM_001015051.3:c.1499G>T NP_001015051.3:p.Ter500Leu
NM_001024630.3:c.1565G>T NP_001019801.3:p.Ter522Leu
NM_001278478.1:c.1457G>T NP_001265407.1:p.Ter486Leu
XM_006715232.1:c.1349G>T XP_006715295.1:p.Ter450Leu
XM_011514960.1:c.1225+34897G>T XP_011513262.1:n.1225+34897G>T
XM_011514961.1:c.1769G>T XP_011513263.1:p.Ter590Leu
XM_011514962.1:c.1703G>T XP_011513264.1:p.Ter568Leu
XM_011514963.1:c.1051+34897G>T XP_011513265.1:n.1051+34897G>T
XM_011514964.1:c.1435+334G>T XP_011513266.1:n.1435+334G>T
XM_011514966.1:c.553+34897G>T XP_011513268.1:n.553+34897G>T
NM_001024630.4:c.1565G>T MANE Select NP_001019801.3:p.Ter522Leu
NM_001278478.2:c.1457G>T NP_001265407.1:p.Ter486Leu
NM_001369405.1:c.1523G>T NP_001356334.1:p.Ter508Leu
NM_001015051.4:c.1499G>T NP_001015051.3:p.Ter500Leu