Canonical Allele Identifier: CA2073001650

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673243G= , CM000674.2:g.132673243G=	GRCh38
NC_000012.11:g.133249829G= , CM000674.1:g.133249829G=	GRCh37
NC_000012.10:g.131759902G=	NCBI36
NG_033840.1:g.19282C= , LRG_789:g.19282C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.102C=
ENST00000545015.2:n.1421C=
ENST00000699982.1:c.1248C=
ENST00000699983.1:c.1248C=
ENST00000699984.1:c.1248C=
ENST00000320574.10:c.1394C= MANE Select	ENSP00000322570.5:p.Ala465=
ENST00000672742.1:c.*896C=	ENSP00000500279.1:n.*896C=
ENST00000320574.9:c.1394C=	ENSP00000322570.5:p.Ala465=
ENST00000535270.5:c.1313C=	ENSP00000445753.1:p.Ala438=
ENST00000535934.2:n.1269C=
ENST00000537064.5:c.*441C=	ENSP00000442578.1:n.*441C=
ENST00000539215.5:n.102C=
NM_006231.3:c.1394C= , LRG_789t1:c.1394C=	NP_006222.2:p.Ala465=
XM_011534795.1:c.1394C=	XP_011533097.1:p.Ala465=
XM_011534796.1:c.1265C=	XP_011533098.1:p.Ala422=
XM_011534797.1:c.473C=	XP_011533099.1:p.Ala158=
XM_011534798.1:c.56C=	XP_011533100.1:p.Ala19=
XM_011534799.1:c.1394C=	XP_011533101.1:p.Ala465=
XM_011534800.1:c.1394C=	XP_011533102.1:p.Ala465=
XM_011534801.1:c.1394C=	XP_011533103.1:p.Ala465=
XR_941395.1:n.1603C=
XM_011534795.3:c.1394C=	XP_011533097.1:p.Ala465=
XM_011534797.3:c.473C=	XP_011533099.1:p.Ala158=
XM_011534799.2:c.1394C=	XP_011533101.1:p.Ala465=
XR_002957338.1:n.1598C=
XR_002957339.1:n.1598C=
XR_941395.2:n.1598C=
NM_006231.4:c.1394C= MANE Select	NP_006222.2:p.Ala465=