Canonical Allele Identifier: CA2073001667

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673267G= , CM000674.2:g.132673267G=	GRCh38
NC_000012.11:g.133249853G= , CM000674.1:g.133249853G=	GRCh37
NC_000012.10:g.131759926G=	NCBI36
NG_033840.1:g.19258C= , LRG_789:g.19258C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.78C=
ENST00000545015.2:n.1397C=
ENST00000699982.1:c.1224C=
ENST00000699983.1:c.1224C=
ENST00000699984.1:c.1224C=
ENST00000320574.10:c.1370C= MANE Select	ENSP00000322570.5:p.Thr457=
ENST00000672742.1:c.*872C=	ENSP00000500279.1:n.*872C=
ENST00000320574.9:c.1370C=	ENSP00000322570.5:p.Thr457=
ENST00000535270.5:c.1289C=	ENSP00000445753.1:p.Thr430=
ENST00000535934.2:n.1245C=
ENST00000537064.5:c.*417C=	ENSP00000442578.1:n.*417C=
ENST00000539215.5:n.78C=
NM_006231.3:c.1370C= , LRG_789t1:c.1370C=	NP_006222.2:p.Thr457=
XM_011534795.1:c.1370C=	XP_011533097.1:p.Thr457=
XM_011534796.1:c.1241C=	XP_011533098.1:p.Thr414=
XM_011534797.1:c.449C=	XP_011533099.1:p.Thr150=
XM_011534798.1:c.32C=	XP_011533100.1:p.Thr11=
XM_011534799.1:c.1370C=	XP_011533101.1:p.Thr457=
XM_011534800.1:c.1370C=	XP_011533102.1:p.Thr457=
XM_011534801.1:c.1370C=	XP_011533103.1:p.Thr457=
XR_941395.1:n.1579C=
XM_011534795.3:c.1370C=	XP_011533097.1:p.Thr457=
XM_011534797.3:c.449C=	XP_011533099.1:p.Thr150=
XM_011534799.2:c.1370C=	XP_011533101.1:p.Thr457=
XR_002957338.1:n.1574C=
XR_002957339.1:n.1574C=
XR_941395.2:n.1574C=
NM_006231.4:c.1370C= MANE Select	NP_006222.2:p.Thr457=