Canonical Allele Identifier: CA2073001611

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673175C= , CM000674.2:g.132673175C=	GRCh38
NC_000012.11:g.133249761C= , CM000674.1:g.133249761C=	GRCh37
NC_000012.10:g.131759834C=	NCBI36
NG_033840.1:g.19350G= , LRG_789:g.19350G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.170G=
ENST00000545015.2:n.1489G=
ENST00000699982.1:c.1316G=
ENST00000699983.1:c.1316G=
ENST00000699984.1:c.1316G=
ENST00000320574.10:c.1462G= MANE Select	ENSP00000322570.5:p.Glu488=
ENST00000672742.1:c.*964G=	ENSP00000500279.1:n.*964G=
ENST00000320574.9:c.1462G=	ENSP00000322570.5:p.Glu488=
ENST00000535270.5:c.1381G=	ENSP00000445753.1:p.Glu461=
ENST00000535934.2:n.1337G=
ENST00000537064.5:c.*509G=	ENSP00000442578.1:n.*509G=
ENST00000539215.5:n.170G=
ENST00000545015.1:n.59G=
NM_006231.3:c.1462G= , LRG_789t1:c.1462G=	NP_006222.2:p.Glu488=
XM_011534795.1:c.1462G=	XP_011533097.1:p.Glu488=
XM_011534796.1:c.1333G=	XP_011533098.1:p.Glu445=
XM_011534797.1:c.541G=	XP_011533099.1:p.Glu181=
XM_011534798.1:c.124G=	XP_011533100.1:p.Glu42=
XM_011534799.1:c.1462G=	XP_011533101.1:p.Glu488=
XM_011534800.1:c.1462G=	XP_011533102.1:p.Glu488=
XM_011534801.1:c.1462G=	XP_011533103.1:p.Glu488=
XR_941395.1:n.1671G=
XM_011534795.3:c.1462G=	XP_011533097.1:p.Glu488=
XM_011534797.3:c.541G=	XP_011533099.1:p.Glu181=
XM_011534799.2:c.1462G=	XP_011533101.1:p.Glu488=
XR_002957338.1:n.1666G=
XR_002957339.1:n.1666G=
XR_941395.2:n.1666G=
NM_006231.4:c.1462G= MANE Select	NP_006222.2:p.Glu488=