Canonical Allele Identifier: CA2073003412

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132676548G= , CM000674.2:g.132676548G=	GRCh38
NC_000012.11:g.133253134G= , CM000674.1:g.133253134G=	GRCh37
NC_000012.10:g.131763207G=	NCBI36
NG_033840.1:g.15977C= , LRG_789:g.15977C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006231.4:c.907C= MANE Select	NP_006222.2:p.Gln303=
ENST00000320574.10:c.907C= MANE Select	ENSP00000322570.5:p.Gln303=
NM_006231.3:c.907C= , LRG_789t1:c.907C=	NP_006222.2:p.Gln303=
ENST00000320574.9:c.907C=	ENSP00000322570.5:p.Gln303=
ENST00000535270.5:c.826C=	ENSP00000445753.1:p.Gln276=
ENST00000537064.5:c.907C=	ENSP00000442578.1:p.Gln303=
ENST00000545015.2:n.934C=
ENST00000672742.1:c.*401C=	ENSP00000500279.1:n.*401C=
ENST00000699982.1:c.753C=
ENST00000699983.1:c.753C=
ENST00000699984.1:c.753C=
XM_011534795.1:c.907C=	XP_011533097.1:p.Gln303=
XM_011534795.3:c.907C=	XP_011533097.1:p.Gln303=
XM_011534796.1:c.778C=	XP_011533098.1:p.Gln260=
XM_011534797.1:c.6C=	XP_011533099.1:p.Ala2=
XM_011534797.3:c.6C=	XP_011533099.1:p.Ala2=
XM_011534799.1:c.907C=	XP_011533101.1:p.Gln303=
XM_011534799.2:c.907C=	XP_011533101.1:p.Gln303=
XM_011534800.1:c.907C=	XP_011533102.1:p.Gln303=
XM_011534801.1:c.907C=	XP_011533103.1:p.Gln303=
XR_002957338.1:n.1111C=
XR_002957339.1:n.1111C=
XR_941395.1:n.1116C=
XR_941395.2:n.1111C=