Canonical Allele Identifier: CA2073001624

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673190T= , CM000674.2:g.132673190T=	GRCh38
NC_000012.11:g.133249776T= , CM000674.1:g.133249776T=	GRCh37
NC_000012.10:g.131759849T=	NCBI36
NG_033840.1:g.19335A= , LRG_789:g.19335A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.155A=
ENST00000545015.2:n.1474A=
ENST00000699982.1:c.1301A=
ENST00000699983.1:c.1301A=
ENST00000699984.1:c.1301A=
ENST00000320574.10:c.1447A= MANE Select	ENSP00000322570.5:p.Thr483=
ENST00000672742.1:c.*949A=	ENSP00000500279.1:n.*949A=
ENST00000320574.9:c.1447A=	ENSP00000322570.5:p.Thr483=
ENST00000535270.5:c.1366A=	ENSP00000445753.1:p.Thr456=
ENST00000535934.2:n.1322A=
ENST00000537064.5:c.*494A=	ENSP00000442578.1:n.*494A=
ENST00000539215.5:n.155A=
ENST00000545015.1:n.44A=
NM_006231.3:c.1447A= , LRG_789t1:c.1447A=	NP_006222.2:p.Thr483=
XM_011534795.1:c.1447A=	XP_011533097.1:p.Thr483=
XM_011534796.1:c.1318A=	XP_011533098.1:p.Thr440=
XM_011534797.1:c.526A=	XP_011533099.1:p.Thr176=
XM_011534798.1:c.109A=	XP_011533100.1:p.Thr37=
XM_011534799.1:c.1447A=	XP_011533101.1:p.Thr483=
XM_011534800.1:c.1447A=	XP_011533102.1:p.Thr483=
XM_011534801.1:c.1447A=	XP_011533103.1:p.Thr483=
XR_941395.1:n.1656A=
XM_011534795.3:c.1447A=	XP_011533097.1:p.Thr483=
XM_011534797.3:c.526A=	XP_011533099.1:p.Thr176=
XM_011534799.2:c.1447A=	XP_011533101.1:p.Thr483=
XR_002957338.1:n.1651A=
XR_002957339.1:n.1651A=
XR_941395.2:n.1651A=
NM_006231.4:c.1447A= MANE Select	NP_006222.2:p.Thr483=