Canonical Allele Identifier: CA2578634963

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45512235C>A , CM000668.2:g.45512235C>A	GRCh38
NC_000006.11:g.45479972C>A , CM000668.1:g.45479972C>A	GRCh37
NC_000006.10:g.45587950C>A	NCBI36
NG_008020.1:g.188919C>A
NG_008020.2:g.188919C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646519.1:c.818-11C>A	ENSP00000496517.1:n.818-11C>A
ENST00000647337.2:c.860-11C>A MANE Select	ENSP00000495497.1:n.860-11C>A
ENST00000359524.7:c.818-11C>A	ENSP00000352514.5:n.818-11C>A
ENST00000371432.7:c.860-11C>A	ENSP00000360486.4:n.860-11C>A
ENST00000371436.10:c.860-11C>A	ENSP00000360491.6:n.860-11C>A
ENST00000371438.5:c.860-11C>A	ENSP00000360493.1:n.860-11C>A
ENST00000465038.6:c.860-11C>A	ENSP00000420707.2:n.860-11C>A
ENST00000478660.6:c.644-11C>A	ENSP00000460188.1:n.644-11C>A
ENST00000483377.5:c.*381-11C>A	ENSP00000461357.1:n.*381-11C>A
ENST00000576263.5:c.860-11C>A	ENSP00000458178.1:n.860-11C>A
ENST00000625924.1:c.818-11C>A	ENSP00000485863.1:n.818-11C>A
NM_001015051.3:c.860-11C>A	NP_001015051.3:n.860-11C>A
NM_001024630.3:c.860-11C>A	NP_001019801.3:n.860-11C>A
NM_001278478.1:c.818-11C>A	NP_001265407.1:n.818-11C>A
XM_006715232.1:c.644-11C>A	XP_006715295.1:n.644-11C>A
XM_011514960.1:c.1064-11C>A	XP_011513262.1:n.1064-11C>A
XM_011514961.1:c.1064-11C>A	XP_011513263.1:n.1064-11C>A
XM_011514962.1:c.1064-11C>A	XP_011513264.1:n.1064-11C>A
XM_011514963.1:c.890-11C>A	XP_011513265.1:n.890-11C>A
XM_011514964.1:c.1064-11C>A	XP_011513266.1:n.1064-11C>A
XM_011514965.1:c.1064-11C>A	XP_011513267.1:n.1064-11C>A
XM_011514966.1:c.392-11C>A	XP_011513268.1:n.392-11C>A
XR_926323.1:n.1658-11C>A
NM_001024630.4:c.860-11C>A MANE Select	NP_001019801.3:n.860-11C>A
NM_001278478.2:c.818-11C>A	NP_001265407.1:n.818-11C>A
NM_001369405.1:c.818-11C>A	NP_001356334.1:n.818-11C>A
NM_001015051.4:c.860-11C>A	NP_001015051.3:n.860-11C>A