Canonical Allele Identifier: CA387359581
Gene: POLE HGNC NCBI

Linked Data

dbSNP Id: rs2136000359

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132673671A>T , CM000674.2:g.132673671A>T GRCh38
NC_000012.11:g.133250257A>T , CM000674.1:g.133250257A>T GRCh37
NC_000012.10:g.131760330A>T NCBI36
NG_033840.1:g.18854T>A , LRG_789:g.18854T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000545015.2:n.1290T>A
ENST00000699982.1:c.1117T>A
ENST00000699983.1:c.1117T>A
ENST00000699984.1:c.1117T>A
ENST00000320574.10:c.1263T>A MANE Select ENSP00000322570.5:p.Ser421Arg
ENST00000672742.1:c.*765T>A ENSP00000500279.1:n.*765T>A
ENST00000320574.9:c.1263T>A ENSP00000322570.5:p.Ser421Arg
ENST00000535270.5:c.1182T>A ENSP00000445753.1:p.Ser394Arg
ENST00000535934.2:n.1138T>A
ENST00000537064.5:c.*310T>A ENSP00000442578.1:n.*310T>A
NM_006231.3:c.1263T>A , LRG_789t1:c.1263T>A NP_006222.2:p.Ser421Arg
XM_011534795.1:c.1263T>A XP_011533097.1:p.Ser421Arg
XM_011534796.1:c.1134T>A XP_011533098.1:p.Ser378Arg
XM_011534797.1:c.342T>A XP_011533099.1:p.Ser114Arg
XM_011534799.1:c.1263T>A XP_011533101.1:p.Ser421Arg
XM_011534800.1:c.1263T>A XP_011533102.1:p.Ser421Arg
XM_011534801.1:c.1263T>A XP_011533103.1:p.Ser421Arg
XR_941395.1:n.1472T>A
XM_011534795.3:c.1263T>A XP_011533097.1:p.Ser421Arg
XM_011534797.3:c.342T>A XP_011533099.1:p.Ser114Arg
XM_011534799.2:c.1263T>A XP_011533101.1:p.Ser421Arg
XR_002957338.1:n.1467T>A
XR_002957339.1:n.1467T>A
XR_941395.2:n.1467T>A
NM_006231.4:c.1263T>A MANE Select NP_006222.2:p.Ser421Arg