Canonical Allele Identifier: CA387356205

Gene: POLE

Linked Data

• MyVariant Identifiers: chr12:g.133248802T>G (hg19) ; chr12:g.132672216T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132672216T>G , CM000674.2:g.132672216T>G	GRCh38
NC_000012.11:g.133248802T>G , CM000674.1:g.133248802T>G	GRCh37
NC_000012.10:g.131758875T>G	NCBI36
NG_033840.1:g.20309A>C , LRG_789:g.20309A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000539215.6:c.548A>C
ENST00000699982.1:c.1647A>C
ENST00000699983.1:c.1647A>C
ENST00000699984.1:c.1647A>C
ENST00000320574.10:c.1793A>C MANE Select	ENSP00000322570.5:p.Glu598Ala
ENST00000672742.1:c.*1295A>C	ENSP00000500279.1:n.*1295A>C
ENST00000320574.9:c.1793A>C	ENSP00000322570.5:p.Glu598Ala
ENST00000535270.5:c.1712A>C	ENSP00000445753.1:p.Glu571Ala
ENST00000537064.5:c.*840A>C	ENSP00000442578.1:n.*840A>C
NM_006231.3:c.1793A>C , LRG_789t1:c.1793A>C	NP_006222.2:p.Glu598Ala
XM_011534795.1:c.1793A>C	XP_011533097.1:p.Glu598Ala
XM_011534796.1:c.1664A>C	XP_011533098.1:p.Glu555Ala
XM_011534797.1:c.872A>C	XP_011533099.1:p.Glu291Ala
XM_011534798.1:c.455A>C	XP_011533100.1:p.Glu152Ala
XM_011534799.1:c.1793A>C	XP_011533101.1:p.Glu598Ala
XM_011534800.1:c.1793A>C	XP_011533102.1:p.Glu598Ala
XM_011534801.1:c.1793A>C	XP_011533103.1:p.Glu598Ala
XR_941395.1:n.2002A>C
XM_011534795.3:c.1793A>C	XP_011533097.1:p.Glu598Ala
XM_011534797.3:c.872A>C	XP_011533099.1:p.Glu291Ala
XM_011534799.2:c.1793A>C	XP_011533101.1:p.Glu598Ala
XR_002957338.1:n.1997A>C
XR_002957339.1:n.1997A>C
XR_941395.2:n.1997A>C
NM_006231.4:c.1793A>C MANE Select	NP_006222.2:p.Glu598Ala