Canonical Allele Identifier: CA387358267

Gene: POLE

Linked Data

• dbSNP Id: rs1418646286
• MyVariant Identifiers: chr12:g.133249785C>G (hg19) ; chr12:g.132673199C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673199C>G , CM000674.2:g.132673199C>G	GRCh38
NC_000012.11:g.133249785C>G , CM000674.1:g.133249785C>G	GRCh37
NC_000012.10:g.131759858C>G	NCBI36
NG_033840.1:g.19326G>C , LRG_789:g.19326G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.146G>C
ENST00000545015.2:n.1465G>C
ENST00000699982.1:c.1292G>C
ENST00000699983.1:c.1292G>C
ENST00000699984.1:c.1292G>C
ENST00000320574.10:c.1438G>C MANE Select	ENSP00000322570.5:p.Ala480Pro
ENST00000672742.1:c.*940G>C	ENSP00000500279.1:n.*940G>C
ENST00000320574.9:c.1438G>C	ENSP00000322570.5:p.Ala480Pro
ENST00000535270.5:c.1357G>C	ENSP00000445753.1:p.Ala453Pro
ENST00000535934.2:n.1313G>C
ENST00000537064.5:c.*485G>C	ENSP00000442578.1:n.*485G>C
ENST00000539215.5:n.146G>C
ENST00000545015.1:n.35G>C
NM_006231.3:c.1438G>C , LRG_789t1:c.1438G>C	NP_006222.2:p.Ala480Pro
XM_011534795.1:c.1438G>C	XP_011533097.1:p.Ala480Pro
XM_011534796.1:c.1309G>C	XP_011533098.1:p.Ala437Pro
XM_011534797.1:c.517G>C	XP_011533099.1:p.Ala173Pro
XM_011534798.1:c.100G>C	XP_011533100.1:p.Ala34Pro
XM_011534799.1:c.1438G>C	XP_011533101.1:p.Ala480Pro
XM_011534800.1:c.1438G>C	XP_011533102.1:p.Ala480Pro
XM_011534801.1:c.1438G>C	XP_011533103.1:p.Ala480Pro
XR_941395.1:n.1647G>C
XM_011534795.3:c.1438G>C	XP_011533097.1:p.Ala480Pro
XM_011534797.3:c.517G>C	XP_011533099.1:p.Ala173Pro
XM_011534799.2:c.1438G>C	XP_011533101.1:p.Ala480Pro
XR_002957338.1:n.1642G>C
XR_002957339.1:n.1642G>C
XR_941395.2:n.1642G>C
NM_006231.4:c.1438G>C MANE Select	NP_006222.2:p.Ala480Pro