Canonical Allele Identifier: CA6893998

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673587C>T , CM000674.2:g.132673587C>T	GRCh38
NC_000012.11:g.133250173C>T , CM000674.1:g.133250173C>T	GRCh37
NC_000012.10:g.131760246C>T	NCBI36
NG_033840.1:g.18938G>A , LRG_789:g.18938G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.55G>A
ENST00000545015.2:n.1374G>A
ENST00000699982.1:c.1201G>A
ENST00000699983.1:c.1201G>A
ENST00000699984.1:c.1201G>A
ENST00000320574.10:c.1347G>A MANE Select	ENSP00000322570.5:p.Thr449=
ENST00000672742.1:c.*849G>A	ENSP00000500279.1:n.*849G>A
ENST00000320574.9:c.1347G>A	ENSP00000322570.5:p.Thr449=
ENST00000535270.5:c.1266G>A	ENSP00000445753.1:p.Thr422=
ENST00000535934.2:n.1222G>A
ENST00000537064.5:c.*394G>A	ENSP00000442578.1:n.*394G>A
ENST00000539215.5:n.55G>A
NM_006231.3:c.1347G>A , LRG_789t1:c.1347G>A	NP_006222.2:p.Thr449=
XM_011534795.1:c.1347G>A	XP_011533097.1:p.Thr449=
XM_011534796.1:c.1218G>A	XP_011533098.1:p.Thr406=
XM_011534797.1:c.426G>A	XP_011533099.1:p.Thr142=
XM_011534798.1:c.-63G>A	XP_011533100.1:n.-63G>A
XM_011534799.1:c.1347G>A	XP_011533101.1:p.Thr449=
XM_011534800.1:c.1347G>A	XP_011533102.1:p.Thr449=
XM_011534801.1:c.1347G>A	XP_011533103.1:p.Thr449=
XR_941395.1:n.1556G>A
XM_011534795.3:c.1347G>A	XP_011533097.1:p.Thr449=
XM_011534797.3:c.426G>A	XP_011533099.1:p.Thr142=
XM_011534799.2:c.1347G>A	XP_011533101.1:p.Thr449=
XR_002957338.1:n.1551G>A
XR_002957339.1:n.1551G>A
XR_941395.2:n.1551G>A
NM_006231.4:c.1347G>A MANE Select	NP_006222.2:p.Thr449=