Canonical Allele Identifier: CA387364277

Gene: POLE

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132676599G>T , CM000674.2:g.132676599G>T	GRCh38
NC_000012.11:g.133253185G>T , CM000674.1:g.133253185G>T	GRCh37
NC_000012.10:g.131763258G>T	NCBI36
NG_033840.1:g.15926C>A , LRG_789:g.15926C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545015.2:n.883C>A
ENST00000699982.1:c.702C>A
ENST00000699983.1:c.702C>A
ENST00000699984.1:c.702C>A
ENST00000320574.10:c.856C>A MANE Select	ENSP00000322570.5:p.Pro286Thr
ENST00000672742.1:c.*350C>A	ENSP00000500279.1:n.*350C>A
ENST00000320574.9:c.856C>A	ENSP00000322570.5:p.Pro286Thr
ENST00000535270.5:c.775C>A	ENSP00000445753.1:p.Pro259Thr
ENST00000537064.5:c.856C>A	ENSP00000442578.1:p.Pro286Thr
NM_006231.3:c.856C>A , LRG_789t1:c.856C>A	NP_006222.2:p.Pro286Thr
XM_011534795.1:c.856C>A	XP_011533097.1:p.Pro286Thr
XM_011534796.1:c.727C>A	XP_011533098.1:p.Pro243Thr
XM_011534797.1:c.-46C>A	XP_011533099.1:n.-46C>A
XM_011534799.1:c.856C>A	XP_011533101.1:p.Pro286Thr
XM_011534800.1:c.856C>A	XP_011533102.1:p.Pro286Thr
XM_011534801.1:c.856C>A	XP_011533103.1:p.Pro286Thr
XR_941395.1:n.1065C>A
XM_011534795.3:c.856C>A	XP_011533097.1:p.Pro286Thr
XM_011534797.3:c.-46C>A	XP_011533099.1:n.-46C>A
XM_011534799.2:c.856C>A	XP_011533101.1:p.Pro286Thr
XR_002957338.1:n.1060C>A
XR_002957339.1:n.1060C>A
XR_941395.2:n.1060C>A
NM_006231.4:c.856C>A MANE Select	NP_006222.2:p.Pro286Thr