Canonical Allele Identifier: CA363957386

Gene: RUNX2

Linked Data

• MyVariant Identifiers: chr6:g.45514987C>T (hg19) ; chr6:g.45547250C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.45547250C>T , CM000668.2:g.45547250C>T	GRCh38
NC_000006.11:g.45514987C>T , CM000668.1:g.45514987C>T	GRCh37
NC_000006.10:g.45622965C>T	NCBI36
NG_008020.1:g.223934C>T
NG_008020.2:g.223934C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646519.1:c.*668C>T	ENSP00000496517.1:n.*668C>T
ENST00000647337.2:c.1511C>T MANE Select	ENSP00000495497.1:p.Pro504Leu
ENST00000359524.7:c.1469C>T	ENSP00000352514.5:p.Pro490Leu
ENST00000371432.7:c.1445C>T	ENSP00000360486.4:p.Pro482Leu
ENST00000371436.10:c.1445C>T	ENSP00000360491.6:p.Pro482Leu
ENST00000371438.5:c.1511C>T	ENSP00000360493.1:p.Pro504Leu
ENST00000465038.6:c.1511C>T	ENSP00000420707.2:p.Pro504Leu
ENST00000478660.6:c.*178+33597C>T	ENSP00000460188.1:n.*178+33597C>T
ENST00000576263.5:c.1021+34843C>T	ENSP00000458178.1:n.1021+34843C>T
ENST00000625924.1:c.1403C>T	ENSP00000485863.1:p.Pro468Leu
NM_001015051.3:c.1445C>T	NP_001015051.3:p.Pro482Leu
NM_001024630.3:c.1511C>T	NP_001019801.3:p.Pro504Leu
NM_001278478.1:c.1403C>T	NP_001265407.1:p.Pro468Leu
XM_006715232.1:c.1295C>T	XP_006715295.1:p.Pro432Leu
XM_011514960.1:c.1225+34843C>T	XP_011513262.1:n.1225+34843C>T
XM_011514961.1:c.1715C>T	XP_011513263.1:p.Pro572Leu
XM_011514962.1:c.1649C>T	XP_011513264.1:p.Pro550Leu
XM_011514963.1:c.1051+34843C>T	XP_011513265.1:n.1051+34843C>T
XM_011514964.1:c.1435+280C>T	XP_011513266.1:n.1435+280C>T
XM_011514966.1:c.553+34843C>T	XP_011513268.1:n.553+34843C>T
NM_001024630.4:c.1511C>T MANE Select	NP_001019801.3:p.Pro504Leu
NM_001278478.2:c.1403C>T	NP_001265407.1:p.Pro468Leu
NM_001369405.1:c.1469C>T	NP_001356334.1:p.Pro490Leu
NM_001015051.4:c.1445C>T	NP_001015051.3:p.Pro482Leu