Canonical Allele Identifier: CA138461118

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45550731C>T , CM000668.2:g.45550731C>T	GRCh38
NC_000006.11:g.45518468C>T , CM000668.1:g.45518468C>T	GRCh37
NC_000006.10:g.45626446C>T	NCBI36
NG_008020.1:g.227415C>T
NG_008020.2:g.227415C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001024630.4:c.*3426C>T MANE Select	NP_001019801.3:n.*3426C>T
ENST00000647337.2:c.*3426C>T MANE Select	ENSP00000495497.1:n.*3426C>T
NM_001015051.3:c.*3426C>T	NP_001015051.3:n.*3426C>T
NM_001015051.4:c.*3426C>T	NP_001015051.3:n.*3426C>T
NM_001024630.3:c.*3426C>T	NP_001019801.3:n.*3426C>T
NM_001278478.1:c.4884C>T	NP_001265407.1:n.4884C>T
NM_001278478.2:c.*3426C>T	NP_001265407.1:n.*3426C>T
NM_001369405.1:c.*3426C>T	NP_001356334.1:n.*3426C>T
ENST00000359524.7:c.*3426C>T	ENSP00000352514.5:n.*3426C>T
ENST00000371432.7:c.*3426C>T	ENSP00000360486.4:n.*3426C>T
ENST00000371438.5:c.*3426C>T	ENSP00000360493.1:n.*3426C>T
ENST00000478660.6:c.*178+37078C>T	ENSP00000460188.1:n.*178+37078C>T
ENST00000576263.5:c.1021+38324C>T	ENSP00000458178.1:n.1021+38324C>T
ENST00000646519.1:c.*4149C>T	ENSP00000496517.1:n.*4149C>T
XM_006715232.1:c.*3426C>T	XP_006715295.1:n.*3426C>T
XM_011514960.1:c.1225+38324C>T	XP_011513262.1:n.1225+38324C>T
XM_011514961.1:c.*3426C>T	XP_011513263.1:n.*3426C>T
XM_011514962.1:c.*3426C>T	XP_011513264.1:n.*3426C>T
XM_011514963.1:c.1051+38324C>T	XP_011513265.1:n.1051+38324C>T
XM_011514964.1:c.*1309C>T	XP_011513266.1:n.*1309C>T
XM_011514966.1:c.553+38324C>T	XP_011513268.1:n.553+38324C>T