Canonical Allele Identifier: CA2073001623

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673189G= , CM000674.2:g.132673189G=	GRCh38
NC_000012.11:g.133249775G= , CM000674.1:g.133249775G=	GRCh37
NC_000012.10:g.131759848G=	NCBI36
NG_033840.1:g.19336C= , LRG_789:g.19336C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.156C=
ENST00000545015.2:n.1475C=
ENST00000699982.1:c.1302C=
ENST00000699983.1:c.1302C=
ENST00000699984.1:c.1302C=
ENST00000320574.10:c.1448C= MANE Select	ENSP00000322570.5:p.Thr483=
ENST00000672742.1:c.*950C=	ENSP00000500279.1:n.*950C=
ENST00000320574.9:c.1448C=	ENSP00000322570.5:p.Thr483=
ENST00000535270.5:c.1367C=	ENSP00000445753.1:p.Thr456=
ENST00000535934.2:n.1323C=
ENST00000537064.5:c.*495C=	ENSP00000442578.1:n.*495C=
ENST00000539215.5:n.156C=
ENST00000545015.1:n.45C=
NM_006231.3:c.1448C= , LRG_789t1:c.1448C=	NP_006222.2:p.Thr483=
XM_011534795.1:c.1448C=	XP_011533097.1:p.Thr483=
XM_011534796.1:c.1319C=	XP_011533098.1:p.Thr440=
XM_011534797.1:c.527C=	XP_011533099.1:p.Thr176=
XM_011534798.1:c.110C=	XP_011533100.1:p.Thr37=
XM_011534799.1:c.1448C=	XP_011533101.1:p.Thr483=
XM_011534800.1:c.1448C=	XP_011533102.1:p.Thr483=
XM_011534801.1:c.1448C=	XP_011533103.1:p.Thr483=
XR_941395.1:n.1657C=
XM_011534795.3:c.1448C=	XP_011533097.1:p.Thr483=
XM_011534797.3:c.527C=	XP_011533099.1:p.Thr176=
XM_011534799.2:c.1448C=	XP_011533101.1:p.Thr483=
XR_002957338.1:n.1652C=
XR_002957339.1:n.1652C=
XR_941395.2:n.1652C=
NM_006231.4:c.1448C= MANE Select	NP_006222.2:p.Thr483=