Canonical Allele Identifier: CA1625492465

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45547299A= , CM000668.2:g.45547299A=	GRCh38
NC_000006.11:g.45515036A= , CM000668.1:g.45515036A=	GRCh37
NC_000006.10:g.45623014A=	NCBI36
NG_008020.1:g.223983A=
NG_008020.2:g.223983A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646519.1:c.*717A=	ENSP00000496517.1:n.*717A=
ENST00000647337.2:c.1560A= MANE Select	ENSP00000495497.1:p.Pro520=
ENST00000359524.7:c.1518A=	ENSP00000352514.5:p.Pro506=
ENST00000371432.7:c.1494A=	ENSP00000360486.4:p.Pro498=
ENST00000371436.10:c.1494A=	ENSP00000360491.6:p.Pro498=
ENST00000371438.5:c.1560A=	ENSP00000360493.1:p.Pro520=
ENST00000465038.6:c.1560A=	ENSP00000420707.2:p.Pro520=
ENST00000478660.6:c.*178+33646A=	ENSP00000460188.1:n.*178+33646A=
ENST00000576263.5:c.1021+34892A=	ENSP00000458178.1:n.1021+34892A=
ENST00000625924.1:c.1452A=	ENSP00000485863.1:p.Pro484=
NM_001015051.3:c.1494A=	NP_001015051.3:p.Pro498=
NM_001024630.3:c.1560A=	NP_001019801.3:p.Pro520=
NM_001278478.1:c.1452A=	NP_001265407.1:p.Pro484=
XM_006715232.1:c.1344A=	XP_006715295.1:p.Pro448=
XM_011514960.1:c.1225+34892A=	XP_011513262.1:n.1225+34892A=
XM_011514961.1:c.1764A=	XP_011513263.1:p.Pro588=
XM_011514962.1:c.1698A=	XP_011513264.1:p.Pro566=
XM_011514963.1:c.1051+34892A=	XP_011513265.1:n.1051+34892A=
XM_011514964.1:c.1435+329A=	XP_011513266.1:n.1435+329A=
XM_011514966.1:c.553+34892A=	XP_011513268.1:n.553+34892A=
NM_001024630.4:c.1560A= MANE Select	NP_001019801.3:p.Pro520=
NM_001278478.2:c.1452A=	NP_001265407.1:p.Pro484=
NM_001369405.1:c.1518A=	NP_001356334.1:p.Pro506=
NM_001015051.4:c.1494A=	NP_001015051.3:p.Pro498=