Canonical Allele Identifier: CA387358756

Gene: POLE

Linked Data

• ClinVar Variation Id: 2836186
• ClinVar RCV Id: RCV003689951
• dbSNP Id: rs765702675
• COSMIC: COSM170809 ; COSM257773
• MyVariant Identifiers: chr12:g.133249847G>A (hg19) ; chr12:g.132673261G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673261G>A , CM000674.2:g.132673261G>A	GRCh38
NC_000012.11:g.133249847G>A , CM000674.1:g.133249847G>A	GRCh37
NC_000012.10:g.131759920G>A	NCBI36
NG_033840.1:g.19264C>T , LRG_789:g.19264C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.84C>T
ENST00000545015.2:n.1403C>T
ENST00000699982.1:c.1230C>T
ENST00000699983.1:c.1230C>T
ENST00000699984.1:c.1230C>T
ENST00000320574.10:c.1376C>T MANE Select	ENSP00000322570.5:p.Ser459Phe
ENST00000672742.1:c.*878C>T	ENSP00000500279.1:n.*878C>T
ENST00000320574.9:c.1376C>T	ENSP00000322570.5:p.Ser459Phe
ENST00000535270.5:c.1295C>T	ENSP00000445753.1:p.Ser432Phe
ENST00000535934.2:n.1251C>T
ENST00000537064.5:c.*423C>T	ENSP00000442578.1:n.*423C>T
ENST00000539215.5:n.84C>T
NM_006231.3:c.1376C>T , LRG_789t1:c.1376C>T	NP_006222.2:p.Ser459Phe
XM_011534795.1:c.1376C>T	XP_011533097.1:p.Ser459Phe
XM_011534796.1:c.1247C>T	XP_011533098.1:p.Ser416Phe
XM_011534797.1:c.455C>T	XP_011533099.1:p.Ser152Phe
XM_011534798.1:c.38C>T	XP_011533100.1:p.Ser13Phe
XM_011534799.1:c.1376C>T	XP_011533101.1:p.Ser459Phe
XM_011534800.1:c.1376C>T	XP_011533102.1:p.Ser459Phe
XM_011534801.1:c.1376C>T	XP_011533103.1:p.Ser459Phe
XR_941395.1:n.1585C>T
XM_011534795.3:c.1376C>T	XP_011533097.1:p.Ser459Phe
XM_011534797.3:c.455C>T	XP_011533099.1:p.Ser152Phe
XM_011534799.2:c.1376C>T	XP_011533101.1:p.Ser459Phe
XR_002957338.1:n.1580C>T
XR_002957339.1:n.1580C>T
XR_941395.2:n.1580C>T
NM_006231.4:c.1376C>T MANE Select	NP_006222.2:p.Ser459Phe