Canonical Allele Identifier: CA566988267

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45530968G>A , CM000668.2:g.45530968G>A	GRCh38
NC_000006.11:g.45498705G>A , CM000668.1:g.45498705G>A	GRCh37
NC_000006.10:g.45606683G>A	NCBI36
NG_008020.1:g.207652G>A
NG_008020.2:g.207652G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001024630.4:c.1022-14249G>A MANE Select	NP_001019801.3:n.1022-14249G>A
ENST00000647337.2:c.1022-14249G>A MANE Select	ENSP00000495497.1:n.1022-14249G>A
NM_001015051.3:c.1022-15859G>A	NP_001015051.3:n.1022-15859G>A
NM_001015051.4:c.1022-15859G>A	NP_001015051.3:n.1022-15859G>A
NM_001024630.3:c.1022-14249G>A	NP_001019801.3:n.1022-14249G>A
NM_001278478.1:c.980-15859G>A	NP_001265407.1:n.980-15859G>A
NM_001278478.2:c.980-15859G>A	NP_001265407.1:n.980-15859G>A
NM_001369405.1:c.980-14249G>A	NP_001356334.1:n.980-14249G>A
ENST00000359524.7:c.980-14249G>A	ENSP00000352514.5:n.980-14249G>A
ENST00000371432.7:c.1022-15859G>A	ENSP00000360486.4:n.1022-15859G>A
ENST00000371436.10:c.1022-15859G>A	ENSP00000360491.6:n.1022-15859G>A
ENST00000371438.5:c.1022-14249G>A	ENSP00000360493.1:n.1022-14249G>A
ENST00000465038.6:c.1022-14249G>A	ENSP00000420707.2:n.1022-14249G>A
ENST00000478660.6:c.*178+17315G>A	ENSP00000460188.1:n.*178+17315G>A
ENST00000483377.5:c.*543-14249G>A	ENSP00000461357.1:n.*543-14249G>A
ENST00000576263.5:c.1021+18561G>A	ENSP00000458178.1:n.1021+18561G>A
ENST00000625924.1:c.980-15859G>A	ENSP00000485863.1:n.980-15859G>A
ENST00000646519.1:c.*179-14249G>A	ENSP00000496517.1:n.*179-14249G>A
XM_006715232.1:c.806-14249G>A	XP_006715295.1:n.806-14249G>A
XM_011514960.1:c.1225+18561G>A	XP_011513262.1:n.1225+18561G>A
XM_011514961.1:c.1226-14249G>A	XP_011513263.1:n.1226-14249G>A
XM_011514962.1:c.1226-15859G>A	XP_011513264.1:n.1226-15859G>A
XM_011514963.1:c.1051+18561G>A	XP_011513265.1:n.1051+18561G>A
XM_011514964.1:c.1226-14249G>A	XP_011513266.1:n.1226-14249G>A
XM_011514966.1:c.553+18561G>A	XP_011513268.1:n.553+18561G>A