Canonical Allele Identifier: CA482849622

Gene: POLE

Linked Data

• dbSNP Id: rs2135990911
• MyVariant Identifiers: chr12:g.133248876C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132672290C>G , CM000674.2:g.132672290C>G	GRCh38
NC_000012.11:g.133248876C>G , CM000674.1:g.133248876C>G	GRCh37
NC_000012.10:g.131758949C>G	NCBI36
NG_033840.1:g.20235G>C , LRG_789:g.20235G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.474G>C
ENST00000699982.1:c.1573G>C
ENST00000699983.1:c.1573G>C
ENST00000699984.1:c.1573G>C
ENST00000320574.10:c.1719G>C MANE Select	ENSP00000322570.5:p.Arg573=
ENST00000672742.1:c.*1221G>C	ENSP00000500279.1:n.*1221G>C
ENST00000320574.9:c.1719G>C	ENSP00000322570.5:p.Arg573=
ENST00000535270.5:c.1638G>C	ENSP00000445753.1:p.Arg546=
ENST00000537064.5:c.*766G>C	ENSP00000442578.1:n.*766G>C
ENST00000539215.5:n.474G>C
NM_006231.3:c.1719G>C , LRG_789t1:c.1719G>C	NP_006222.2:p.Arg573=
XM_011534795.1:c.1719G>C	XP_011533097.1:p.Arg573=
XM_011534796.1:c.1590G>C	XP_011533098.1:p.Arg530=
XM_011534797.1:c.798G>C	XP_011533099.1:p.Arg266=
XM_011534798.1:c.381G>C	XP_011533100.1:p.Arg127=
XM_011534799.1:c.1719G>C	XP_011533101.1:p.Arg573=
XM_011534800.1:c.1719G>C	XP_011533102.1:p.Arg573=
XM_011534801.1:c.1719G>C	XP_011533103.1:p.Arg573=
XR_941395.1:n.1928G>C
XM_011534795.3:c.1719G>C	XP_011533097.1:p.Arg573=
XM_011534797.3:c.798G>C	XP_011533099.1:p.Arg266=
XM_011534799.2:c.1719G>C	XP_011533101.1:p.Arg573=
XR_002957338.1:n.1923G>C
XR_002957339.1:n.1923G>C
XR_941395.2:n.1923G>C
NM_006231.4:c.1719G>C MANE Select	NP_006222.2:p.Arg573=