Canonical Allele Identifier: CA2073001617

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673181G= , CM000674.2:g.132673181G=	GRCh38
NC_000012.11:g.133249767G= , CM000674.1:g.133249767G=	GRCh37
NC_000012.10:g.131759840G=	NCBI36
NG_033840.1:g.19344C= , LRG_789:g.19344C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.164C=
ENST00000545015.2:n.1483C=
ENST00000699982.1:c.1310C=
ENST00000699983.1:c.1310C=
ENST00000699984.1:c.1310C=
ENST00000320574.10:c.1456C= MANE Select	ENSP00000322570.5:p.Pro486=
ENST00000672742.1:c.*958C=	ENSP00000500279.1:n.*958C=
ENST00000320574.9:c.1456C=	ENSP00000322570.5:p.Pro486=
ENST00000535270.5:c.1375C=	ENSP00000445753.1:p.Pro459=
ENST00000535934.2:n.1331C=
ENST00000537064.5:c.*503C=	ENSP00000442578.1:n.*503C=
ENST00000539215.5:n.164C=
ENST00000545015.1:n.53C=
NM_006231.3:c.1456C= , LRG_789t1:c.1456C=	NP_006222.2:p.Pro486=
XM_011534795.1:c.1456C=	XP_011533097.1:p.Pro486=
XM_011534796.1:c.1327C=	XP_011533098.1:p.Pro443=
XM_011534797.1:c.535C=	XP_011533099.1:p.Pro179=
XM_011534798.1:c.118C=	XP_011533100.1:p.Pro40=
XM_011534799.1:c.1456C=	XP_011533101.1:p.Pro486=
XM_011534800.1:c.1456C=	XP_011533102.1:p.Pro486=
XM_011534801.1:c.1456C=	XP_011533103.1:p.Pro486=
XR_941395.1:n.1665C=
XM_011534795.3:c.1456C=	XP_011533097.1:p.Pro486=
XM_011534797.3:c.535C=	XP_011533099.1:p.Pro179=
XM_011534799.2:c.1456C=	XP_011533101.1:p.Pro486=
XR_002957338.1:n.1660C=
XR_002957339.1:n.1660C=
XR_941395.2:n.1660C=
NM_006231.4:c.1456C= MANE Select	NP_006222.2:p.Pro486=