Canonical Allele Identifier: CA10626986

Gene: RUNX2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45550465G>T , CM000668.2:g.45550465G>T	GRCh38
NC_000006.11:g.45518202G>T , CM000668.1:g.45518202G>T	GRCh37
NC_000006.10:g.45626180G>T	NCBI36
NG_008020.1:g.227149G>T
NG_008020.2:g.227149G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001024630.4:c.*3160G>T MANE Select	NP_001019801.3:n.*3160G>T
ENST00000647337.2:c.*3160G>T MANE Select	ENSP00000495497.1:n.*3160G>T
NM_001015051.3:c.*3160G>T	NP_001015051.3:n.*3160G>T
NM_001015051.4:c.*3160G>T	NP_001015051.3:n.*3160G>T
NM_001024630.3:c.*3160G>T	NP_001019801.3:n.*3160G>T
NM_001278478.1:c.4618G>T	NP_001265407.1:n.4618G>T
NM_001278478.2:c.*3160G>T	NP_001265407.1:n.*3160G>T
NM_001369405.1:c.*3160G>T	NP_001356334.1:n.*3160G>T
ENST00000359524.7:c.*3160G>T	ENSP00000352514.5:n.*3160G>T
ENST00000371432.7:c.*3160G>T	ENSP00000360486.4:n.*3160G>T
ENST00000371438.5:c.*3160G>T	ENSP00000360493.1:n.*3160G>T
ENST00000478660.6:c.*178+36812G>T	ENSP00000460188.1:n.*178+36812G>T
ENST00000576263.5:c.1021+38058G>T	ENSP00000458178.1:n.1021+38058G>T
ENST00000646519.1:c.*3883G>T	ENSP00000496517.1:n.*3883G>T
XM_006715232.1:c.*3160G>T	XP_006715295.1:n.*3160G>T
XM_011514960.1:c.1225+38058G>T	XP_011513262.1:n.1225+38058G>T
XM_011514961.1:c.*3160G>T	XP_011513263.1:n.*3160G>T
XM_011514962.1:c.*3160G>T	XP_011513264.1:n.*3160G>T
XM_011514963.1:c.1051+38058G>T	XP_011513265.1:n.1051+38058G>T
XM_011514964.1:c.*1043G>T	XP_011513266.1:n.*1043G>T
XM_011514966.1:c.553+38058G>T	XP_011513268.1:n.553+38058G>T