Canonical Allele Identifier: CA482722677

Gene: POLE

Linked Data

• ClinVar Variation Id: 1087558
• ClinVar RCV Id: RCV003656991
• dbSNP Id: rs2135996166
• MyVariant Identifiers: chr12:g.133249795T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673209T>C , CM000674.2:g.132673209T>C	GRCh38
NC_000012.11:g.133249795T>C , CM000674.1:g.133249795T>C	GRCh37
NC_000012.10:g.131759868T>C	NCBI36
NG_033840.1:g.19316A>G , LRG_789:g.19316A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.136A>G
ENST00000545015.2:n.1455A>G
ENST00000699982.1:c.1282A>G
ENST00000699983.1:c.1282A>G
ENST00000699984.1:c.1282A>G
ENST00000320574.10:c.1428A>G MANE Select	ENSP00000322570.5:p.Pro476=
ENST00000672742.1:c.*930A>G	ENSP00000500279.1:n.*930A>G
ENST00000320574.9:c.1428A>G	ENSP00000322570.5:p.Pro476=
ENST00000535270.5:c.1347A>G	ENSP00000445753.1:p.Pro449=
ENST00000535934.2:n.1303A>G
ENST00000537064.5:c.*475A>G	ENSP00000442578.1:n.*475A>G
ENST00000539215.5:n.136A>G
ENST00000545015.1:n.25A>G
NM_006231.3:c.1428A>G , LRG_789t1:c.1428A>G	NP_006222.2:p.Pro476=
XM_011534795.1:c.1428A>G	XP_011533097.1:p.Pro476=
XM_011534796.1:c.1299A>G	XP_011533098.1:p.Pro433=
XM_011534797.1:c.507A>G	XP_011533099.1:p.Pro169=
XM_011534798.1:c.90A>G	XP_011533100.1:p.Pro30=
XM_011534799.1:c.1428A>G	XP_011533101.1:p.Pro476=
XM_011534800.1:c.1428A>G	XP_011533102.1:p.Pro476=
XM_011534801.1:c.1428A>G	XP_011533103.1:p.Pro476=
XR_941395.1:n.1637A>G
XM_011534795.3:c.1428A>G	XP_011533097.1:p.Pro476=
XM_011534797.3:c.507A>G	XP_011533099.1:p.Pro169=
XM_011534799.2:c.1428A>G	XP_011533101.1:p.Pro476=
XR_002957338.1:n.1632A>G
XR_002957339.1:n.1632A>G
XR_941395.2:n.1632A>G
NM_006231.4:c.1428A>G MANE Select	NP_006222.2:p.Pro476=