Canonical Allele Identifier: CA1625471244

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45497905_45497909delinsCTGTT , CM000668.2:g.45497905_45497909delinsCTGTT	GRCh38
NC_000006.11:g.45465642_45465646delinsCTGTT , CM000668.1:g.45465642_45465646delinsCTGTT	GRCh37
NC_000006.10:g.45573620_45573624delinsCTGTT	NCBI36
NG_008020.1:g.174589_174593delinsCTGTT
NG_008020.2:g.174589_174593delinsCTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646519.1:c.817+5791_817+5795delinsCTGTT	ENSP00000496517.1:n.817+5791_817+5795delinsCTGTT
ENST00000647337.2:c.859+5791_859+5795delinsCTGTT MANE Select	ENSP00000495497.1:n.859+5791_859+5795delinsCTGTT
ENST00000359524.7:c.817+5791_817+5795delinsCTGTT	ENSP00000352514.5:n.817+5791_817+5795delinsCTGTT
ENST00000371432.7:c.859+5791_859+5795delinsCTGTT	ENSP00000360486.4:n.859+5791_859+5795delinsCTGTT
ENST00000371436.10:c.859+5791_859+5795delinsCTGTT	ENSP00000360491.6:n.859+5791_859+5795delinsCTGTT
ENST00000371438.5:c.859+5791_859+5795delinsCTGTT	ENSP00000360493.1:n.859+5791_859+5795delinsCTGTT
ENST00000465038.6:c.859+5791_859+5795delinsCTGTT	ENSP00000420707.2:n.859+5791_859+5795delinsCTGTT
ENST00000478660.6:c.644-14341_644-14337delinsCTGTT	ENSP00000460188.1:n.644-14341_644-14337delinsCTGTT
ENST00000483377.5:c.*380+5791_*380+5795delinsCTGTT	ENSP00000461357.1:n.*380+5791_*380+5795delinsCTGTT
ENST00000576263.5:c.859+5791_859+5795delinsCTGTT	ENSP00000458178.1:n.859+5791_859+5795delinsCTGTT
ENST00000625924.1:c.817+5791_817+5795delinsCTGTT	ENSP00000485863.1:n.817+5791_817+5795delinsCTGTT
NM_001015051.3:c.859+5791_859+5795delinsCTGTT	NP_001015051.3:n.859+5791_859+5795delinsCTGTT
NM_001024630.3:c.859+5791_859+5795delinsCTGTT	NP_001019801.3:n.859+5791_859+5795delinsCTGTT
NM_001278478.1:c.817+5791_817+5795delinsCTGTT	NP_001265407.1:n.817+5791_817+5795delinsCTGTT
XM_006715232.1:c.644-14341_644-14337delinsCTGTT	XP_006715295.1:n.644-14341_644-14337delinsCTGTT
XM_011514960.1:c.1063+5791_1063+5795delinsCTGTT	XP_011513262.1:n.1063+5791_1063+5795delinsCTGTT
XM_011514961.1:c.1063+5791_1063+5795delinsCTGTT	XP_011513263.1:n.1063+5791_1063+5795delinsCTGTT
XM_011514962.1:c.1063+5791_1063+5795delinsCTGTT	XP_011513264.1:n.1063+5791_1063+5795delinsCTGTT
XM_011514963.1:c.890-14341_890-14337delinsCTGTT	XP_011513265.1:n.890-14341_890-14337delinsCTGTT
XM_011514964.1:c.1063+5791_1063+5795delinsCTGTT	XP_011513266.1:n.1063+5791_1063+5795delinsCTGTT
XM_011514965.1:c.1063+5791_1063+5795delinsCTGTT	XP_011513267.1:n.1063+5791_1063+5795delinsCTGTT
XM_011514966.1:c.391+5791_391+5795delinsCTGTT	XP_011513268.1:n.391+5791_391+5795delinsCTGTT
XR_926323.1:n.1657+4943_1657+4947delinsCTGTT
NM_001024630.4:c.859+5791_859+5795delinsCTGTT MANE Select	NP_001019801.3:n.859+5791_859+5795delinsCTGTT
NM_001278478.2:c.817+5791_817+5795delinsCTGTT	NP_001265407.1:n.817+5791_817+5795delinsCTGTT
NM_001369405.1:c.817+5791_817+5795delinsCTGTT	NP_001356334.1:n.817+5791_817+5795delinsCTGTT
NM_001015051.4:c.859+5791_859+5795delinsCTGTT	NP_001015051.3:n.859+5791_859+5795delinsCTGTT