Canonical Allele Identifier: CA1625492535

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45547461T= , CM000668.2:g.45547461T=	GRCh38
NC_000006.11:g.45515198T= , CM000668.1:g.45515198T=	GRCh37
NC_000006.10:g.45623176T=	NCBI36
NG_008020.1:g.224145T=
NG_008020.2:g.224145T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646519.1:c.*879T=	ENSP00000496517.1:n.*879T=
ENST00000647337.2:c.*156T= MANE Select	ENSP00000495497.1:n.*156T=
ENST00000359524.7:c.*156T=	ENSP00000352514.5:n.*156T=
ENST00000371432.7:c.*156T=	ENSP00000360486.4:n.*156T=
ENST00000371438.5:c.*156T=	ENSP00000360493.1:n.*156T=
ENST00000478660.6:c.*178+33808T=	ENSP00000460188.1:n.*178+33808T=
ENST00000576263.5:c.1021+35054T=	ENSP00000458178.1:n.1021+35054T=
NM_001015051.3:c.*156T=	NP_001015051.3:n.*156T=
NM_001024630.3:c.*156T=	NP_001019801.3:n.*156T=
NM_001278478.1:c.1614T=	NP_001265407.1:n.1614T=
XM_006715232.1:c.*156T=	XP_006715295.1:n.*156T=
XM_011514960.1:c.1225+35054T=	XP_011513262.1:n.1225+35054T=
XM_011514961.1:c.*156T=	XP_011513263.1:n.*156T=
XM_011514962.1:c.*156T=	XP_011513264.1:n.*156T=
XM_011514963.1:c.1051+35054T=	XP_011513265.1:n.1051+35054T=
XM_011514964.1:c.1435+491T=	XP_011513266.1:n.1435+491T=
XM_011514966.1:c.553+35054T=	XP_011513268.1:n.553+35054T=
NM_001024630.4:c.*156T= MANE Select	NP_001019801.3:n.*156T=
NM_001278478.2:c.*156T=	NP_001265407.1:n.*156T=
NM_001369405.1:c.*156T=	NP_001356334.1:n.*156T=
NM_001015051.4:c.*156T=	NP_001015051.3:n.*156T=