Canonical Allele Identifier: CA2073001572

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673117G= , CM000674.2:g.132673117G=	GRCh38
NC_000012.11:g.133249703G= , CM000674.1:g.133249703G=	GRCh37
NC_000012.10:g.131759776G=	NCBI36
NG_033840.1:g.19408C= , LRG_789:g.19408C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.181+47C=
ENST00000545015.2:n.1500+47C=
ENST00000699982.1:c.1327+47C=
ENST00000699983.1:c.1327+47C=
ENST00000699984.1:c.1327+47C=
ENST00000320574.10:c.1473+47C= MANE Select	ENSP00000322570.5:n.1473+47C=
ENST00000672742.1:c.*975+47C=	ENSP00000500279.1:n.*975+47C=
ENST00000320574.9:c.1473+47C=	ENSP00000322570.5:n.1473+47C=
ENST00000535270.5:c.1392+47C=	ENSP00000445753.1:n.1392+47C=
ENST00000535934.2:n.1348+47C=
ENST00000537064.5:c.*520+47C=	ENSP00000442578.1:n.*520+47C=
ENST00000539215.5:n.181+47C=
ENST00000545015.1:n.70+47C=
NM_006231.3:c.1473+47C= , LRG_789t1:c.1473+47C=	NP_006222.2:n.1473+47C=
XM_011534795.1:c.1473+47C=	XP_011533097.1:n.1473+47C=
XM_011534796.1:c.1344+47C=	XP_011533098.1:n.1344+47C=
XM_011534797.1:c.552+47C=	XP_011533099.1:n.552+47C=
XM_011534798.1:c.135+47C=	XP_011533100.1:n.135+47C=
XM_011534799.1:c.1473+47C=	XP_011533101.1:n.1473+47C=
XM_011534800.1:c.1473+47C=	XP_011533102.1:n.1473+47C=
XM_011534801.1:c.1473+47C=	XP_011533103.1:n.1473+47C=
XR_941395.1:n.1682+47C=
XM_011534795.3:c.1473+47C=	XP_011533097.1:n.1473+47C=
XM_011534797.3:c.552+47C=	XP_011533099.1:n.552+47C=
XM_011534799.2:c.1473+47C=	XP_011533101.1:n.1473+47C=
XR_002957338.1:n.1677+47C=
XR_002957339.1:n.1677+47C=
XR_941395.2:n.1677+47C=
NM_006231.4:c.1473+47C= MANE Select	NP_006222.2:n.1473+47C=