Canonical Allele Identifier: CA1625471245

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45497906T= , CM000668.2:g.45497906T=	GRCh38
NC_000006.11:g.45465643T= , CM000668.1:g.45465643T=	GRCh37
NC_000006.10:g.45573621T=	NCBI36
NG_008020.1:g.174590T=
NG_008020.2:g.174590T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646519.1:c.817+5792T=	ENSP00000496517.1:n.817+5792T=
ENST00000647337.2:c.859+5792T= MANE Select	ENSP00000495497.1:n.859+5792T=
ENST00000359524.7:c.817+5792T=	ENSP00000352514.5:n.817+5792T=
ENST00000371432.7:c.859+5792T=	ENSP00000360486.4:n.859+5792T=
ENST00000371436.10:c.859+5792T=	ENSP00000360491.6:n.859+5792T=
ENST00000371438.5:c.859+5792T=	ENSP00000360493.1:n.859+5792T=
ENST00000465038.6:c.859+5792T=	ENSP00000420707.2:n.859+5792T=
ENST00000478660.6:c.644-14340T=	ENSP00000460188.1:n.644-14340T=
ENST00000483377.5:c.*380+5792T=	ENSP00000461357.1:n.*380+5792T=
ENST00000576263.5:c.859+5792T=	ENSP00000458178.1:n.859+5792T=
ENST00000625924.1:c.817+5792T=	ENSP00000485863.1:n.817+5792T=
NM_001015051.3:c.859+5792T=	NP_001015051.3:n.859+5792T=
NM_001024630.3:c.859+5792T=	NP_001019801.3:n.859+5792T=
NM_001278478.1:c.817+5792T=	NP_001265407.1:n.817+5792T=
XM_006715232.1:c.644-14340T=	XP_006715295.1:n.644-14340T=
XM_011514960.1:c.1063+5792T=	XP_011513262.1:n.1063+5792T=
XM_011514961.1:c.1063+5792T=	XP_011513263.1:n.1063+5792T=
XM_011514962.1:c.1063+5792T=	XP_011513264.1:n.1063+5792T=
XM_011514963.1:c.890-14340T=	XP_011513265.1:n.890-14340T=
XM_011514964.1:c.1063+5792T=	XP_011513266.1:n.1063+5792T=
XM_011514965.1:c.1063+5792T=	XP_011513267.1:n.1063+5792T=
XM_011514966.1:c.391+5792T=	XP_011513268.1:n.391+5792T=
XR_926323.1:n.1657+4944T=
NM_001024630.4:c.859+5792T= MANE Select	NP_001019801.3:n.859+5792T=
NM_001278478.2:c.817+5792T=	NP_001265407.1:n.817+5792T=
NM_001369405.1:c.817+5792T=	NP_001356334.1:n.817+5792T=
NM_001015051.4:c.859+5792T=	NP_001015051.3:n.859+5792T=