Canonical Allele Identifier: CA387355634

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132668932T>A , CM000674.2:g.132668932T>A	GRCh38
NC_000012.11:g.133245518T>A , CM000674.1:g.133245518T>A	GRCh37
NC_000012.10:g.131755591T>A	NCBI36
NG_033840.1:g.23593A>T , LRG_789:g.23593A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006231.4:c.1802A>T MANE Select	NP_006222.2:p.Asp601Val
ENST00000320574.10:c.1802A>T MANE Select	ENSP00000322570.5:p.Asp601Val
NM_006231.3:c.1802A>T , LRG_789t1:c.1802A>T	NP_006222.2:p.Asp601Val
ENST00000320574.9:c.1802A>T	ENSP00000322570.5:p.Asp601Val
ENST00000535270.5:c.1721A>T	ENSP00000445753.1:p.Asp574Val
ENST00000537064.5:c.*849A>T	ENSP00000442578.1:n.*849A>T
ENST00000539215.6:c.557A>T
ENST00000672742.1:c.*1304A>T	ENSP00000500279.1:n.*1304A>T
ENST00000699982.1:c.1656A>T
ENST00000699983.1:c.1656A>T
ENST00000699984.1:c.1656A>T
XM_011534795.1:c.1802A>T	XP_011533097.1:p.Asp601Val
XM_011534795.3:c.1802A>T	XP_011533097.1:p.Asp601Val
XM_011534796.1:c.1673A>T	XP_011533098.1:p.Asp558Val
XM_011534797.1:c.881A>T	XP_011533099.1:p.Asp294Val
XM_011534797.3:c.881A>T	XP_011533099.1:p.Asp294Val
XM_011534798.1:c.464A>T	XP_011533100.1:p.Asp155Val
XM_011534799.1:c.1802A>T	XP_011533101.1:p.Asp601Val
XM_011534799.2:c.1802A>T	XP_011533101.1:p.Asp601Val
XM_011534800.1:c.1802A>T	XP_011533102.1:p.Asp601Val
XM_011534801.1:c.1802A>T	XP_011533103.1:p.Asp601Val
XR_002957338.1:n.2006A>T
XR_002957339.1:n.2006A>T
XR_941395.1:n.2011A>T
XR_941395.2:n.2006A>T