Canonical Allele Identifier: CA450348167

Gene: RUNX2

Linked Data

• MyVariant Identifiers: chr6:g.45514952T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45547215T>C , CM000668.2:g.45547215T>C	GRCh38
NC_000006.11:g.45514952T>C , CM000668.1:g.45514952T>C	GRCh37
NC_000006.10:g.45622930T>C	NCBI36
NG_008020.1:g.223899T>C
NG_008020.2:g.223899T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646519.1:c.*633T>C	ENSP00000496517.1:n.*633T>C
ENST00000647337.2:c.1476T>C MANE Select	ENSP00000495497.1:p.Asp492=
ENST00000359524.7:c.1434T>C	ENSP00000352514.5:p.Asp478=
ENST00000371432.7:c.1410T>C	ENSP00000360486.4:p.Asp470=
ENST00000371436.10:c.1410T>C	ENSP00000360491.6:p.Asp470=
ENST00000371438.5:c.1476T>C	ENSP00000360493.1:p.Asp492=
ENST00000465038.6:c.1476T>C	ENSP00000420707.2:p.Asp492=
ENST00000478660.6:c.*178+33562T>C	ENSP00000460188.1:n.*178+33562T>C
ENST00000576263.5:c.1021+34808T>C	ENSP00000458178.1:n.1021+34808T>C
ENST00000625924.1:c.1368T>C	ENSP00000485863.1:p.Asp456=
NM_001015051.3:c.1410T>C	NP_001015051.3:p.Asp470=
NM_001024630.3:c.1476T>C	NP_001019801.3:p.Asp492=
NM_001278478.1:c.1368T>C	NP_001265407.1:p.Asp456=
XM_006715232.1:c.1260T>C	XP_006715295.1:p.Asp420=
XM_011514960.1:c.1225+34808T>C	XP_011513262.1:n.1225+34808T>C
XM_011514961.1:c.1680T>C	XP_011513263.1:p.Asp560=
XM_011514962.1:c.1614T>C	XP_011513264.1:p.Asp538=
XM_011514963.1:c.1051+34808T>C	XP_011513265.1:n.1051+34808T>C
XM_011514964.1:c.1435+245T>C	XP_011513266.1:n.1435+245T>C
XM_011514966.1:c.553+34808T>C	XP_011513268.1:n.553+34808T>C
NM_001024630.4:c.1476T>C MANE Select	NP_001019801.3:p.Asp492=
NM_001278478.2:c.1368T>C	NP_001265407.1:p.Asp456=
NM_001369405.1:c.1434T>C	NP_001356334.1:p.Asp478=
NM_001015051.4:c.1410T>C	NP_001015051.3:p.Asp470=