Canonical Allele Identifier: CA387358713
Gene: POLE HGNC NCBI

Linked Data

dbSNP Id: rs2135996800

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132673255G>C , CM000674.2:g.132673255G>C GRCh38
NC_000012.11:g.133249841G>C , CM000674.1:g.133249841G>C GRCh37
NC_000012.10:g.131759914G>C NCBI36
NG_033840.1:g.19270C>G , LRG_789:g.19270C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000539215.6:c.90C>G
ENST00000545015.2:n.1409C>G
ENST00000699982.1:c.1236C>G
ENST00000699983.1:c.1236C>G
ENST00000699984.1:c.1236C>G
ENST00000320574.10:c.1382C>G MANE Select ENSP00000322570.5:p.Ser461Ter
ENST00000672742.1:c.*884C>G ENSP00000500279.1:n.*884C>G
ENST00000320574.9:c.1382C>G ENSP00000322570.5:p.Ser461Ter
ENST00000535270.5:c.1301C>G ENSP00000445753.1:p.Ser434Ter
ENST00000535934.2:n.1257C>G
ENST00000537064.5:c.*429C>G ENSP00000442578.1:n.*429C>G
ENST00000539215.5:n.90C>G
NM_006231.3:c.1382C>G , LRG_789t1:c.1382C>G NP_006222.2:p.Ser461Ter
XM_011534795.1:c.1382C>G XP_011533097.1:p.Ser461Ter
XM_011534796.1:c.1253C>G XP_011533098.1:p.Ser418Ter
XM_011534797.1:c.461C>G XP_011533099.1:p.Ser154Ter
XM_011534798.1:c.44C>G XP_011533100.1:p.Ser15Ter
XM_011534799.1:c.1382C>G XP_011533101.1:p.Ser461Ter
XM_011534800.1:c.1382C>G XP_011533102.1:p.Ser461Ter
XM_011534801.1:c.1382C>G XP_011533103.1:p.Ser461Ter
XR_941395.1:n.1591C>G
XM_011534795.3:c.1382C>G XP_011533097.1:p.Ser461Ter
XM_011534797.3:c.461C>G XP_011533099.1:p.Ser154Ter
XM_011534799.2:c.1382C>G XP_011533101.1:p.Ser461Ter
XR_002957338.1:n.1586C>G
XR_002957339.1:n.1586C>G
XR_941395.2:n.1586C>G
NM_006231.4:c.1382C>G MANE Select NP_006222.2:p.Ser461Ter