Canonical Allele Identifier: CA2840507062

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673164dup , CM000674.2:g.132673164dup	GRCh38
NC_000012.11:g.133249750dup , CM000674.1:g.133249750dup	GRCh37
NC_000012.10:g.131759823dup	NCBI36
NG_033840.1:g.19362dup , LRG_789:g.19362dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.181+1dup
ENST00000545015.2:n.1500+1dup
ENST00000699982.1:c.1327+1dup
ENST00000699983.1:c.1327+1dup
ENST00000699984.1:c.1327+1dup
ENST00000320574.10:c.1473+1dup
ENST00000672742.1:c.*975+1dup
ENST00000320574.9:c.1473+1dup
ENST00000535270.5:c.1392+1dup
ENST00000535934.2:n.1348+1dup
ENST00000537064.5:c.*520+1dup
ENST00000539215.5:n.181+1dup
ENST00000545015.1:n.70+1dup
NM_006231.3:c.1473+1dup , LRG_789t1:c.1473+1dup
XM_011534795.1:c.1473+1dup
XM_011534796.1:c.1344+1dup
XM_011534797.1:c.552+1dup
XM_011534798.1:c.135+1dup
XM_011534799.1:c.1473+1dup
XM_011534800.1:c.1473+1dup
XM_011534801.1:c.1473+1dup
XR_941395.1:n.1682+1dup
XM_011534795.3:c.1473+1dup
XM_011534797.3:c.552+1dup
XM_011534799.2:c.1473+1dup
XR_002957338.1:n.1677+1dup
XR_002957339.1:n.1677+1dup
XR_941395.2:n.1677+1dup
NM_006231.4:c.1473+1dup