Canonical Allele Identifier: CA2073001654

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673247C= , CM000674.2:g.132673247C=	GRCh38
NC_000012.11:g.133249833C= , CM000674.1:g.133249833C=	GRCh37
NC_000012.10:g.131759906C=	NCBI36
NG_033840.1:g.19278G= , LRG_789:g.19278G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.98G=
ENST00000545015.2:n.1417G=
ENST00000699982.1:c.1244G=
ENST00000699983.1:c.1244G=
ENST00000699984.1:c.1244G=
ENST00000320574.10:c.1390G= MANE Select	ENSP00000322570.5:p.Val464=
ENST00000672742.1:c.*892G=	ENSP00000500279.1:n.*892G=
ENST00000320574.9:c.1390G=	ENSP00000322570.5:p.Val464=
ENST00000535270.5:c.1309G=	ENSP00000445753.1:p.Val437=
ENST00000535934.2:n.1265G=
ENST00000537064.5:c.*437G=	ENSP00000442578.1:n.*437G=
ENST00000539215.5:n.98G=
NM_006231.3:c.1390G= , LRG_789t1:c.1390G=	NP_006222.2:p.Val464=
XM_011534795.1:c.1390G=	XP_011533097.1:p.Val464=
XM_011534796.1:c.1261G=	XP_011533098.1:p.Val421=
XM_011534797.1:c.469G=	XP_011533099.1:p.Val157=
XM_011534798.1:c.52G=	XP_011533100.1:p.Val18=
XM_011534799.1:c.1390G=	XP_011533101.1:p.Val464=
XM_011534800.1:c.1390G=	XP_011533102.1:p.Val464=
XM_011534801.1:c.1390G=	XP_011533103.1:p.Val464=
XR_941395.1:n.1599G=
XM_011534795.3:c.1390G=	XP_011533097.1:p.Val464=
XM_011534797.3:c.469G=	XP_011533099.1:p.Val157=
XM_011534799.2:c.1390G=	XP_011533101.1:p.Val464=
XR_002957338.1:n.1594G=
XR_002957339.1:n.1594G=
XR_941395.2:n.1594G=
NM_006231.4:c.1390G= MANE Select	NP_006222.2:p.Val464=