Canonical Allele Identifier: CA2073003222

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132676159C= , CM000674.2:g.132676159C=	GRCh38
NC_000012.11:g.133252745C= , CM000674.1:g.133252745C=	GRCh37
NC_000012.10:g.131762818C=	NCBI36
NG_033840.1:g.16366G= , LRG_789:g.16366G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006231.4:c.955G= MANE Select	NP_006222.2:p.Asp319=
ENST00000320574.10:c.955G= MANE Select	ENSP00000322570.5:p.Asp319=
NM_006231.3:c.955G= , LRG_789t1:c.955G=	NP_006222.2:p.Asp319=
ENST00000320574.9:c.955G=	ENSP00000322570.5:p.Asp319=
ENST00000535270.5:c.874G=	ENSP00000445753.1:p.Asp292=
ENST00000535934.2:n.340G=
ENST00000537064.5:c.*2G=	ENSP00000442578.1:n.*2G=
ENST00000545015.2:n.982G=
ENST00000672742.1:c.*449G=	ENSP00000500279.1:n.*449G=
ENST00000699982.1:c.801G=
ENST00000699983.1:c.801G=
ENST00000699984.1:c.801G=
XM_011534795.1:c.955G=	XP_011533097.1:p.Asp319=
XM_011534795.3:c.955G=	XP_011533097.1:p.Asp319=
XM_011534796.1:c.826G=	XP_011533098.1:p.Asp276=
XM_011534797.1:c.34G=	XP_011533099.1:p.Asp12=
XM_011534797.3:c.34G=	XP_011533099.1:p.Asp12=
XM_011534799.1:c.955G=	XP_011533101.1:p.Asp319=
XM_011534799.2:c.955G=	XP_011533101.1:p.Asp319=
XM_011534800.1:c.955G=	XP_011533102.1:p.Asp319=
XM_011534801.1:c.955G=	XP_011533103.1:p.Asp319=
XR_002957338.1:n.1159G=
XR_002957339.1:n.1159G=
XR_941395.1:n.1164G=
XR_941395.2:n.1159G=