Canonical Allele Identifier: CA2073001060
Gene: POLE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132672222A= , CM000674.2:g.132672222A= GRCh38
NC_000012.11:g.133248808A= , CM000674.1:g.133248808A= GRCh37
NC_000012.10:g.131758881A= NCBI36
NG_033840.1:g.20303T= , LRG_789:g.20303T=

Transcript Alleles

HGVS Amino-acid change
ENST00000539215.6:c.542T=
ENST00000699982.1:c.1641T=
ENST00000699983.1:c.1641T=
ENST00000699984.1:c.1641T=
ENST00000320574.10:c.1787T= MANE Select ENSP00000322570.5:p.Phe596=
ENST00000672742.1:c.*1289T= ENSP00000500279.1:n.*1289T=
ENST00000320574.9:c.1787T= ENSP00000322570.5:p.Phe596=
ENST00000535270.5:c.1706T= ENSP00000445753.1:p.Phe569=
ENST00000537064.5:c.*834T= ENSP00000442578.1:n.*834T=
NM_006231.3:c.1787T= , LRG_789t1:c.1787T= NP_006222.2:p.Phe596=
XM_011534795.1:c.1787T= XP_011533097.1:p.Phe596=
XM_011534796.1:c.1658T= XP_011533098.1:p.Phe553=
XM_011534797.1:c.866T= XP_011533099.1:p.Phe289=
XM_011534798.1:c.449T= XP_011533100.1:p.Phe150=
XM_011534799.1:c.1787T= XP_011533101.1:p.Phe596=
XM_011534800.1:c.1787T= XP_011533102.1:p.Phe596=
XM_011534801.1:c.1787T= XP_011533103.1:p.Phe596=
XR_941395.1:n.1996T=
XM_011534795.3:c.1787T= XP_011533097.1:p.Phe596=
XM_011534797.3:c.866T= XP_011533099.1:p.Phe289=
XM_011534799.2:c.1787T= XP_011533101.1:p.Phe596=
XR_002957338.1:n.1991T=
XR_002957339.1:n.1991T=
XR_941395.2:n.1991T=
NM_006231.4:c.1787T= MANE Select NP_006222.2:p.Phe596=