Canonical Allele Identifier: CA685553782
Gene: POLE HGNC NCBI

Linked Data

dbSNP Id: rs1484110381

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132672098_132672099del , CM000674.2:g.132672098_132672099del GRCh38
NC_000012.11:g.133248684_133248685del , CM000674.1:g.133248684_133248685del GRCh37
NC_000012.10:g.131758757_131758758del NCBI36
NG_033840.1:g.20429_20430del , LRG_789:g.20429_20430del

Transcript Alleles

HGVS Amino-acid Change
ENST00000539215.6:c.549+119_549+120del
ENST00000699982.1:c.1648+119_1648+120del
ENST00000699983.1:c.1648+119_1648+120del
ENST00000699984.1:c.1648+119_1648+120del
ENST00000320574.10:c.1794+119_1794+120del MANE Select ENSP00000322570.5:n.1794+119_1794+120del
ENST00000672742.1:c.*1296+119_*1296+120del ENSP00000500279.1:n.*1296+119_*1296+120del
ENST00000320574.9:c.1794+119_1794+120del ENSP00000322570.5:n.1794+119_1794+120del
ENST00000535270.5:c.1713+119_1713+120del ENSP00000445753.1:n.1713+119_1713+120del
ENST00000537064.5:c.*841+119_*841+120del ENSP00000442578.1:n.*841+119_*841+120del
NM_006231.3:c.1794+119_1794+120del , LRG_789t1:c.1794+119_1794+120del NP_006222.2:n.1794+119_1794+120del
XM_011534795.1:c.1794+119_1794+120del XP_011533097.1:n.1794+119_1794+120del
XM_011534796.1:c.1665+119_1665+120del XP_011533098.1:n.1665+119_1665+120del
XM_011534797.1:c.873+119_873+120del XP_011533099.1:n.873+119_873+120del
XM_011534798.1:c.456+119_456+120del XP_011533100.1:n.456+119_456+120del
XM_011534799.1:c.1794+119_1794+120del XP_011533101.1:n.1794+119_1794+120del
XM_011534800.1:c.1794+119_1794+120del XP_011533102.1:n.1794+119_1794+120del
XM_011534801.1:c.1794+119_1794+120del XP_011533103.1:n.1794+119_1794+120del
XR_941395.1:n.2003+119_2003+120del
XM_011534795.3:c.1794+119_1794+120del XP_011533097.1:n.1794+119_1794+120del
XM_011534797.3:c.873+119_873+120del XP_011533099.1:n.873+119_873+120del
XM_011534799.2:c.1794+119_1794+120del XP_011533101.1:n.1794+119_1794+120del
XR_002957338.1:n.1998+119_1998+120del
XR_002957339.1:n.1998+119_1998+120del
XR_941395.2:n.1998+119_1998+120del
NM_006231.4:c.1794+119_1794+120del MANE Select NP_006222.2:n.1794+119_1794+120del