Canonical Allele Identifier: CA825107757

Gene: RUNX2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45457203A>T , CM000668.2:g.45457203A>T	GRCh38
NC_000006.11:g.45424940A>T , CM000668.1:g.45424940A>T	GRCh37
NC_000006.10:g.45532918A>T	NCBI36
NG_008020.1:g.133887A>T
NG_008020.2:g.133887A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646519.1:c.643+19152A>T	ENSP00000496517.1:n.643+19152A>T
ENST00000647337.2:c.685+19152A>T MANE Select	ENSP00000495497.1:n.685+19152A>T
ENST00000359524.7:c.643+19152A>T	ENSP00000352514.5:n.643+19152A>T
ENST00000371432.7:c.685+19152A>T	ENSP00000360486.4:n.685+19152A>T
ENST00000371436.10:c.685+19152A>T	ENSP00000360491.6:n.685+19152A>T
ENST00000371438.5:c.685+19152A>T	ENSP00000360493.1:n.685+19152A>T
ENST00000465038.6:c.685+19152A>T	ENSP00000420707.2:n.685+19152A>T
ENST00000478660.6:c.643+19152A>T	ENSP00000460188.1:n.643+19152A>T
ENST00000483377.5:c.*206+19152A>T	ENSP00000461357.1:n.*206+19152A>T
ENST00000576263.5:c.685+19152A>T	ENSP00000458178.1:n.685+19152A>T
ENST00000625924.1:c.643+19152A>T	ENSP00000485863.1:n.643+19152A>T
NM_001015051.3:c.685+19152A>T	NP_001015051.3:n.685+19152A>T
NM_001024630.3:c.685+19152A>T	NP_001019801.3:n.685+19152A>T
NM_001278478.1:c.643+19152A>T	NP_001265407.1:n.643+19152A>T
XM_006715232.1:c.643+19152A>T	XP_006715295.1:n.643+19152A>T
XM_011514960.1:c.889+19152A>T	XP_011513262.1:n.889+19152A>T
XM_011514961.1:c.889+19152A>T	XP_011513263.1:n.889+19152A>T
XM_011514962.1:c.889+19152A>T	XP_011513264.1:n.889+19152A>T
XM_011514963.1:c.889+19152A>T	XP_011513265.1:n.889+19152A>T
XM_011514964.1:c.889+19152A>T	XP_011513266.1:n.889+19152A>T
XM_011514965.1:c.889+19152A>T	XP_011513267.1:n.889+19152A>T
XM_011514966.1:c.217+19152A>T	XP_011513268.1:n.217+19152A>T
XM_011514967.1:c.972+18506A>T	XP_011513269.1:n.972+18506A>T
XM_011514968.1:c.890-13121A>T	XP_011513270.1:n.890-13121A>T
XR_926323.1:n.1401+19152A>T
NM_001024630.4:c.685+19152A>T MANE Select	NP_001019801.3:n.685+19152A>T
NM_001278478.2:c.643+19152A>T	NP_001265407.1:n.643+19152A>T
NM_001369405.1:c.643+19152A>T	NP_001356334.1:n.643+19152A>T
NM_001015051.4:c.685+19152A>T	NP_001015051.3:n.685+19152A>T