Canonical Allele Identifier: CA387359564

Gene: POLE

Linked Data

• ClinVar Variation Id: 1764317
• ClinVar RCV Id: RCV002373388
• dbSNP Id: rs2136000304
• MyVariant Identifiers: chr12:g.133250254A>T (hg19) ; chr12:g.132673668A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673668A>T , CM000674.2:g.132673668A>T	GRCh38
NC_000012.11:g.133250254A>T , CM000674.1:g.133250254A>T	GRCh37
NC_000012.10:g.131760327A>T	NCBI36
NG_033840.1:g.18857T>A , LRG_789:g.18857T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000545015.2:n.1293T>A
ENST00000699982.1:c.1120T>A
ENST00000699983.1:c.1120T>A
ENST00000699984.1:c.1120T>A
ENST00000320574.10:c.1266T>A MANE Select	ENSP00000322570.5:p.His422Gln
ENST00000672742.1:c.*768T>A	ENSP00000500279.1:n.*768T>A
ENST00000320574.9:c.1266T>A	ENSP00000322570.5:p.His422Gln
ENST00000535270.5:c.1185T>A	ENSP00000445753.1:p.His395Gln
ENST00000535934.2:n.1141T>A
ENST00000537064.5:c.*313T>A	ENSP00000442578.1:n.*313T>A
NM_006231.3:c.1266T>A , LRG_789t1:c.1266T>A	NP_006222.2:p.His422Gln
XM_011534795.1:c.1266T>A	XP_011533097.1:p.His422Gln
XM_011534796.1:c.1137T>A	XP_011533098.1:p.His379Gln
XM_011534797.1:c.345T>A	XP_011533099.1:p.His115Gln
XM_011534799.1:c.1266T>A	XP_011533101.1:p.His422Gln
XM_011534800.1:c.1266T>A	XP_011533102.1:p.His422Gln
XM_011534801.1:c.1266T>A	XP_011533103.1:p.His422Gln
XR_941395.1:n.1475T>A
XM_011534795.3:c.1266T>A	XP_011533097.1:p.His422Gln
XM_011534797.3:c.345T>A	XP_011533099.1:p.His115Gln
XM_011534799.2:c.1266T>A	XP_011533101.1:p.His422Gln
XR_002957338.1:n.1470T>A
XR_002957339.1:n.1470T>A
XR_941395.2:n.1470T>A
NM_006231.4:c.1266T>A MANE Select	NP_006222.2:p.His422Gln