Canonical Allele Identifier: CA692858

Gene: RUNX3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.24902256C>T , CM000663.2:g.24902256C>T	GRCh38
NC_000001.10:g.25228747C>T , CM000663.1:g.25228747C>T	GRCh37
NC_000001.9:g.25101334C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004350.3:c.1114G>A MANE Select	NP_004341.1:p.Ala372Thr
ENST00000308873.11:c.1114G>A MANE Select	ENSP00000308051.6:p.Ala372Thr
NM_001031680.2:c.1156G>A	NP_001026850.1:p.Ala386Thr
NM_001320672.1:c.1156G>A	NP_001307601.1:p.Ala386Thr
NM_004350.2:c.1114G>A	NP_004341.1:p.Ala372Thr
ENST00000308873.10:c.1114G>A	ENSP00000308051.6:p.Ala372Thr
ENST00000338888.3:c.1156G>A	ENSP00000343477.3:p.Ala386Thr
ENST00000338888.4:c.1156G>A	ENSP00000343477.3:p.Ala386Thr
ENST00000399916.5:c.1156G>A	ENSP00000382800.1:p.Ala386Thr
XM_005246024.3:c.1156G>A	XP_005246081.1:p.Ala386Thr
XM_005246024.4:c.1156G>A	XP_005246081.1:p.Ala386Thr
XM_011542351.1:c.997G>A	XP_011540653.1:p.Ala333Thr