Canonical Allele Identifier: CA3836413

Gene: RUNX2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45431945G>A , CM000668.2:g.45431945G>A	GRCh38
NC_000006.11:g.45399682G>A , CM000668.1:g.45399682G>A	GRCh37
NC_000006.10:g.45507660G>A	NCBI36
NG_008020.1:g.108629G>A
NG_008020.2:g.108629G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646519.1:c.464G>A	ENSP00000496517.1:p.Arg155Gln
ENST00000647337.2:c.506G>A MANE Select	ENSP00000495497.1:p.Arg169Gln
ENST00000359524.7:c.464G>A	ENSP00000352514.5:p.Arg155Gln
ENST00000371432.7:c.506G>A	ENSP00000360486.4:p.Arg169Gln
ENST00000371436.10:c.506G>A	ENSP00000360491.6:p.Arg169Gln
ENST00000371438.5:c.506G>A	ENSP00000360493.1:p.Arg169Gln
ENST00000465038.6:c.506G>A	ENSP00000420707.2:p.Arg169Gln
ENST00000478660.6:c.464G>A	ENSP00000460188.1:p.Arg155Gln
ENST00000483377.5:c.*27G>A	ENSP00000461357.1:n.*27G>A
ENST00000576263.5:c.506G>A	ENSP00000458178.1:p.Arg169Gln
ENST00000625924.1:c.464G>A	ENSP00000485863.1:p.Arg155Gln
NM_001015051.3:c.506G>A	NP_001015051.3:p.Arg169Gln
NM_001024630.3:c.506G>A	NP_001019801.3:p.Arg169Gln
NM_001278478.1:c.464G>A	NP_001265407.1:p.Arg155Gln
XM_006715232.1:c.464G>A	XP_006715295.1:p.Arg155Gln
XM_011514960.1:c.710G>A	XP_011513262.1:p.Arg237Gln
XM_011514961.1:c.710G>A	XP_011513263.1:p.Arg237Gln
XM_011514962.1:c.710G>A	XP_011513264.1:p.Arg237Gln
XM_011514963.1:c.710G>A	XP_011513265.1:p.Arg237Gln
XM_011514964.1:c.710G>A	XP_011513266.1:p.Arg237Gln
XM_011514965.1:c.710G>A	XP_011513267.1:p.Arg237Gln
XM_011514966.1:c.38G>A	XP_011513268.1:p.Arg13Gln
XM_011514967.1:c.710G>A	XP_011513269.1:p.Arg237Gln
XM_011514968.1:c.710G>A	XP_011513270.1:p.Arg237Gln
XR_926323.1:n.1222G>A
NM_001024630.4:c.506G>A MANE Select	NP_001019801.3:p.Arg169Gln
NM_001278478.2:c.464G>A	NP_001265407.1:p.Arg155Gln
NM_001369405.1:c.464G>A	NP_001356334.1:p.Arg155Gln
NM_001015051.4:c.506G>A	NP_001015051.3:p.Arg169Gln