Canonical Allele Identifier: CA2073001056
Gene: POLE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132672215C= , CM000674.2:g.132672215C= GRCh38
NC_000012.11:g.133248801C= , CM000674.1:g.133248801C= GRCh37
NC_000012.10:g.131758874C= NCBI36
NG_033840.1:g.20310G= , LRG_789:g.20310G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000539215.6:c.549G=
ENST00000699982.1:c.1648G=
ENST00000699983.1:c.1648G=
ENST00000699984.1:c.1648G=
ENST00000320574.10:c.1794G= MANE Select ENSP00000322570.5:p.Glu598=
ENST00000672742.1:c.*1296G= ENSP00000500279.1:n.*1296G=
ENST00000320574.9:c.1794G= ENSP00000322570.5:p.Glu598=
ENST00000535270.5:c.1713G= ENSP00000445753.1:p.Glu571=
ENST00000537064.5:c.*841G= ENSP00000442578.1:n.*841G=
NM_006231.3:c.1794G= , LRG_789t1:c.1794G= NP_006222.2:p.Glu598=
XM_011534795.1:c.1794G= XP_011533097.1:p.Glu598=
XM_011534796.1:c.1665G= XP_011533098.1:p.Glu555=
XM_011534797.1:c.873G= XP_011533099.1:p.Glu291=
XM_011534798.1:c.456G= XP_011533100.1:p.Glu152=
XM_011534799.1:c.1794G= XP_011533101.1:p.Glu598=
XM_011534800.1:c.1794G= XP_011533102.1:p.Glu598=
XM_011534801.1:c.1794G= XP_011533103.1:p.Glu598=
XR_941395.1:n.2003G=
XM_011534795.3:c.1794G= XP_011533097.1:p.Glu598=
XM_011534797.3:c.873G= XP_011533099.1:p.Glu291=
XM_011534799.2:c.1794G= XP_011533101.1:p.Glu598=
XR_002957338.1:n.1998G=
XR_002957339.1:n.1998G=
XR_941395.2:n.1998G=
NM_006231.4:c.1794G= MANE Select NP_006222.2:p.Glu598=