Canonical Allele Identifier: CA1625492489

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45547356T= , CM000668.2:g.45547356T=	GRCh38
NC_000006.11:g.45515093T= , CM000668.1:g.45515093T=	GRCh37
NC_000006.10:g.45623071T=	NCBI36
NG_008020.1:g.224040T=
NG_008020.2:g.224040T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646519.1:c.*774T=	ENSP00000496517.1:n.*774T=
ENST00000647337.2:c.*51T= MANE Select	ENSP00000495497.1:n.*51T=
ENST00000359524.7:c.*51T=	ENSP00000352514.5:n.*51T=
ENST00000371432.7:c.*51T=	ENSP00000360486.4:n.*51T=
ENST00000371436.10:c.1551T=	ENSP00000360491.6:n.1551T=
ENST00000371438.5:c.*51T=	ENSP00000360493.1:n.*51T=
ENST00000478660.6:c.*178+33703T=	ENSP00000460188.1:n.*178+33703T=
ENST00000576263.5:c.1021+34949T=	ENSP00000458178.1:n.1021+34949T=
NM_001015051.3:c.*51T=	NP_001015051.3:n.*51T=
NM_001024630.3:c.*51T=	NP_001019801.3:n.*51T=
NM_001278478.1:c.1509T=	NP_001265407.1:n.1509T=
XM_006715232.1:c.*51T=	XP_006715295.1:n.*51T=
XM_011514960.1:c.1225+34949T=	XP_011513262.1:n.1225+34949T=
XM_011514961.1:c.*51T=	XP_011513263.1:n.*51T=
XM_011514962.1:c.*51T=	XP_011513264.1:n.*51T=
XM_011514963.1:c.1051+34949T=	XP_011513265.1:n.1051+34949T=
XM_011514964.1:c.1435+386T=	XP_011513266.1:n.1435+386T=
XM_011514966.1:c.553+34949T=	XP_011513268.1:n.553+34949T=
NM_001024630.4:c.*51T= MANE Select	NP_001019801.3:n.*51T=
NM_001278478.2:c.*51T=	NP_001265407.1:n.*51T=
NM_001369405.1:c.*51T=	NP_001356334.1:n.*51T=
NM_001015051.4:c.*51T=	NP_001015051.3:n.*51T=