Canonical Allele Identifier: CA387364285

Gene: POLE

Linked Data

• dbSNP Id: rs2136015916
• MyVariant Identifiers: chr12:g.133253188A>T (hg19) ; chr12:g.132676602A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132676602A>T , CM000674.2:g.132676602A>T	GRCh38
NC_000012.11:g.133253188A>T , CM000674.1:g.133253188A>T	GRCh37
NC_000012.10:g.131763261A>T	NCBI36
NG_033840.1:g.15923T>A , LRG_789:g.15923T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000545015.2:n.880T>A
ENST00000699982.1:c.699T>A
ENST00000699983.1:c.699T>A
ENST00000699984.1:c.699T>A
ENST00000320574.10:c.853T>A MANE Select	ENSP00000322570.5:p.Phe285Ile
ENST00000672742.1:c.*347T>A	ENSP00000500279.1:n.*347T>A
ENST00000320574.9:c.853T>A	ENSP00000322570.5:p.Phe285Ile
ENST00000535270.5:c.772T>A	ENSP00000445753.1:p.Phe258Ile
ENST00000537064.5:c.853T>A	ENSP00000442578.1:p.Phe285Ile
NM_006231.3:c.853T>A , LRG_789t1:c.853T>A	NP_006222.2:p.Phe285Ile
XM_011534795.1:c.853T>A	XP_011533097.1:p.Phe285Ile
XM_011534796.1:c.724T>A	XP_011533098.1:p.Phe242Ile
XM_011534797.1:c.-49T>A	XP_011533099.1:n.-49T>A
XM_011534799.1:c.853T>A	XP_011533101.1:p.Phe285Ile
XM_011534800.1:c.853T>A	XP_011533102.1:p.Phe285Ile
XM_011534801.1:c.853T>A	XP_011533103.1:p.Phe285Ile
XR_941395.1:n.1062T>A
XM_011534795.3:c.853T>A	XP_011533097.1:p.Phe285Ile
XM_011534797.3:c.-49T>A	XP_011533099.1:n.-49T>A
XM_011534799.2:c.853T>A	XP_011533101.1:p.Phe285Ile
XR_002957338.1:n.1057T>A
XR_002957339.1:n.1057T>A
XR_941395.2:n.1057T>A
NM_006231.4:c.853T>A MANE Select	NP_006222.2:p.Phe285Ile