Canonical Allele Identifier: CA482722816

Gene: POLE

Linked Data

• dbSNP Id: rs2136000304
• MyVariant Identifiers: chr12:g.133250254A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673668A>G , CM000674.2:g.132673668A>G	GRCh38
NC_000012.11:g.133250254A>G , CM000674.1:g.133250254A>G	GRCh37
NC_000012.10:g.131760327A>G	NCBI36
NG_033840.1:g.18857T>C , LRG_789:g.18857T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545015.2:n.1293T>C
ENST00000699982.1:c.1120T>C
ENST00000699983.1:c.1120T>C
ENST00000699984.1:c.1120T>C
ENST00000320574.10:c.1266T>C MANE Select	ENSP00000322570.5:p.His422=
ENST00000672742.1:c.*768T>C	ENSP00000500279.1:n.*768T>C
ENST00000320574.9:c.1266T>C	ENSP00000322570.5:p.His422=
ENST00000535270.5:c.1185T>C	ENSP00000445753.1:p.His395=
ENST00000535934.2:n.1141T>C
ENST00000537064.5:c.*313T>C	ENSP00000442578.1:n.*313T>C
NM_006231.3:c.1266T>C , LRG_789t1:c.1266T>C	NP_006222.2:p.His422=
XM_011534795.1:c.1266T>C	XP_011533097.1:p.His422=
XM_011534796.1:c.1137T>C	XP_011533098.1:p.His379=
XM_011534797.1:c.345T>C	XP_011533099.1:p.His115=
XM_011534799.1:c.1266T>C	XP_011533101.1:p.His422=
XM_011534800.1:c.1266T>C	XP_011533102.1:p.His422=
XM_011534801.1:c.1266T>C	XP_011533103.1:p.His422=
XR_941395.1:n.1475T>C
XM_011534795.3:c.1266T>C	XP_011533097.1:p.His422=
XM_011534797.3:c.345T>C	XP_011533099.1:p.His115=
XM_011534799.2:c.1266T>C	XP_011533101.1:p.His422=
XR_002957338.1:n.1470T>C
XR_002957339.1:n.1470T>C
XR_941395.2:n.1470T>C
NM_006231.4:c.1266T>C MANE Select	NP_006222.2:p.His422=