Canonical Allele Identifier: CA363955883

Gene: RUNX2

Linked Data

• gnomAD v4: 6-45512273-C-G
• MyVariant Identifiers: chr6:g.45480010C>G (hg19) ; chr6:g.45512273C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45512273C>G , CM000668.2:g.45512273C>G	GRCh38
NC_000006.11:g.45480010C>G , CM000668.1:g.45480010C>G	GRCh37
NC_000006.10:g.45587988C>G	NCBI36
NG_008020.1:g.188957C>G
NG_008020.2:g.188957C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646519.1:c.845C>G	ENSP00000496517.1:p.Pro282Arg
ENST00000647337.2:c.887C>G MANE Select	ENSP00000495497.1:p.Pro296Arg
ENST00000359524.7:c.845C>G	ENSP00000352514.5:p.Pro282Arg
ENST00000371432.7:c.887C>G	ENSP00000360486.4:p.Pro296Arg
ENST00000371436.10:c.887C>G	ENSP00000360491.6:p.Pro296Arg
ENST00000371438.5:c.887C>G	ENSP00000360493.1:p.Pro296Arg
ENST00000465038.6:c.887C>G	ENSP00000420707.2:p.Pro296Arg
ENST00000478660.6:c.671C>G	ENSP00000460188.1:p.Pro224Arg
ENST00000483377.5:c.*408C>G	ENSP00000461357.1:n.*408C>G
ENST00000576263.5:c.887C>G	ENSP00000458178.1:p.Pro296Arg
ENST00000625924.1:c.845C>G	ENSP00000485863.1:p.Pro282Arg
NM_001015051.3:c.887C>G	NP_001015051.3:p.Pro296Arg
NM_001024630.3:c.887C>G	NP_001019801.3:p.Pro296Arg
NM_001278478.1:c.845C>G	NP_001265407.1:p.Pro282Arg
XM_006715232.1:c.671C>G	XP_006715295.1:p.Pro224Arg
XM_011514960.1:c.1091C>G	XP_011513262.1:p.Pro364Arg
XM_011514961.1:c.1091C>G	XP_011513263.1:p.Pro364Arg
XM_011514962.1:c.1091C>G	XP_011513264.1:p.Pro364Arg
XM_011514963.1:c.917C>G	XP_011513265.1:p.Pro306Arg
XM_011514964.1:c.1091C>G	XP_011513266.1:p.Pro364Arg
XM_011514965.1:c.1091C>G	XP_011513267.1:p.Pro364Arg
XM_011514966.1:c.419C>G	XP_011513268.1:p.Pro140Arg
XR_926323.1:n.1685C>G
NM_001024630.4:c.887C>G MANE Select	NP_001019801.3:p.Pro296Arg
NM_001278478.2:c.845C>G	NP_001265407.1:p.Pro282Arg
NM_001369405.1:c.845C>G	NP_001356334.1:p.Pro282Arg
NM_001015051.4:c.887C>G	NP_001015051.3:p.Pro296Arg