Canonical Allele Identifier: CA6892176

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132626202C>A , CM000674.2:g.132626202C>A	GRCh38
NC_000012.11:g.133202788C>A , CM000674.1:g.133202788C>A	GRCh37
NC_000012.10:g.131712861C>A	NCBI36
NG_033840.1:g.66323G>T , LRG_789:g.66323G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434528.5:c.1984G>T	ENSP00000500921.1:n.1984G>T
ENST00000534922.6:n.359G>T
ENST00000544870.6:c.4099G>T	ENSP00000479927.2:n.4099G>T
ENST00000699981.1:n.4100G>T
ENST00000699982.1:c.6300G>T
ENST00000699983.1:c.7004G>T
ENST00000699984.1:c.6232G>T
ENST00000320574.10:c.6446G>T MANE Select	ENSP00000322570.5:p.Arg2149Leu
ENST00000434528.4:c.1984G>T	ENSP00000500921.1:n.1984G>T
ENST00000672002.1:c.4119G>T	ENSP00000500233.1:n.4119G>T
ENST00000672742.1:c.*6652G>T	ENSP00000500279.1:n.*6652G>T
ENST00000320574.9:c.6446G>T	ENSP00000322570.5:p.Arg2149Leu
ENST00000534922.5:n.359G>T
ENST00000535270.5:c.6365G>T	ENSP00000445753.1:p.Arg2122Leu
ENST00000537064.5:c.*6197G>T	ENSP00000442578.1:n.*6197G>T
ENST00000538196.1:n.218G>T
ENST00000544692.5:n.1815G>T
NM_006231.3:c.6446G>T , LRG_789t1:c.6446G>T	NP_006222.2:p.Arg2149Leu
XM_011534795.1:c.6446G>T	XP_011533097.1:p.Arg2149Leu
XM_011534796.1:c.6317G>T	XP_011533098.1:p.Arg2106Leu
XM_011534797.1:c.5525G>T	XP_011533099.1:p.Arg1842Leu
XM_011534798.1:c.5108G>T	XP_011533100.1:p.Arg1703Leu
XM_011534802.1:c.3434G>T	XP_011533104.1:p.Arg1145Leu
XM_011534795.3:c.6446G>T	XP_011533097.1:p.Arg2149Leu
XM_011534797.3:c.5525G>T	XP_011533099.1:p.Arg1842Leu
XM_011534802.3:c.3434G>T	XP_011533104.1:p.Arg1145Leu
XR_002957339.1:n.6992G>T
NM_006231.4:c.6446G>T MANE Select	NP_006222.2:p.Arg2149Leu