Canonical Allele Identifier: CA387359763

Gene: POLE

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673703C>T , CM000674.2:g.132673703C>T	GRCh38
NC_000012.11:g.133250289C>T , CM000674.1:g.133250289C>T	GRCh37
NC_000012.10:g.131760362C>T	NCBI36
NG_033840.1:g.18822G>A , LRG_789:g.18822G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545015.2:n.1258G>A
ENST00000699982.1:c.1085G>A
ENST00000699983.1:c.1085G>A
ENST00000699984.1:c.1085G>A
ENST00000320574.10:c.1231G>A MANE Select	ENSP00000322570.5:p.Val411Met
ENST00000672742.1:c.*733G>A	ENSP00000500279.1:n.*733G>A
ENST00000320574.9:c.1231G>A	ENSP00000322570.5:p.Val411Met
ENST00000535270.5:c.1150G>A	ENSP00000445753.1:p.Val384Met
ENST00000535934.2:n.1106G>A
ENST00000537064.5:c.*278G>A	ENSP00000442578.1:n.*278G>A
NM_006231.3:c.1231G>A , LRG_789t1:c.1231G>A	NP_006222.2:p.Val411Met
XM_011534795.1:c.1231G>A	XP_011533097.1:p.Val411Met
XM_011534796.1:c.1102G>A	XP_011533098.1:p.Val368Met
XM_011534797.1:c.310G>A	XP_011533099.1:p.Val104Met
XM_011534799.1:c.1231G>A	XP_011533101.1:p.Val411Met
XM_011534800.1:c.1231G>A	XP_011533102.1:p.Val411Met
XM_011534801.1:c.1231G>A	XP_011533103.1:p.Val411Met
XR_941395.1:n.1440G>A
XM_011534795.3:c.1231G>A	XP_011533097.1:p.Val411Met
XM_011534797.3:c.310G>A	XP_011533099.1:p.Val104Met
XM_011534799.2:c.1231G>A	XP_011533101.1:p.Val411Met
XR_002957338.1:n.1435G>A
XR_002957339.1:n.1435G>A
XR_941395.2:n.1435G>A
NM_006231.4:c.1231G>A MANE Select	NP_006222.2:p.Val411Met