Canonical Allele Identifier: CA2073003434
Gene: POLE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132676599G= , CM000674.2:g.132676599G= GRCh38
NC_000012.11:g.133253185G= , CM000674.1:g.133253185G= GRCh37
NC_000012.10:g.131763258G= NCBI36
NG_033840.1:g.15926C= , LRG_789:g.15926C=

Transcript Alleles

HGVS Amino-acid change
ENST00000545015.2:n.883C=
ENST00000699982.1:c.702C=
ENST00000699983.1:c.702C=
ENST00000699984.1:c.702C=
ENST00000320574.10:c.856C= MANE Select ENSP00000322570.5:p.Pro286=
ENST00000672742.1:c.*350C= ENSP00000500279.1:n.*350C=
ENST00000320574.9:c.856C= ENSP00000322570.5:p.Pro286=
ENST00000535270.5:c.775C= ENSP00000445753.1:p.Pro259=
ENST00000537064.5:c.856C= ENSP00000442578.1:p.Pro286=
NM_006231.3:c.856C= , LRG_789t1:c.856C= NP_006222.2:p.Pro286=
XM_011534795.1:c.856C= XP_011533097.1:p.Pro286=
XM_011534796.1:c.727C= XP_011533098.1:p.Pro243=
XM_011534797.1:c.-46C= XP_011533099.1:n.-46C=
XM_011534799.1:c.856C= XP_011533101.1:p.Pro286=
XM_011534800.1:c.856C= XP_011533102.1:p.Pro286=
XM_011534801.1:c.856C= XP_011533103.1:p.Pro286=
XR_941395.1:n.1065C=
XM_011534795.3:c.856C= XP_011533097.1:p.Pro286=
XM_011534797.3:c.-46C= XP_011533099.1:n.-46C=
XM_011534799.2:c.856C= XP_011533101.1:p.Pro286=
XR_002957338.1:n.1060C=
XR_002957339.1:n.1060C=
XR_941395.2:n.1060C=
NM_006231.4:c.856C= MANE Select NP_006222.2:p.Pro286=