Canonical Allele Identifier: CA2622059705
Gene: POLE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132673145_132673147del , CM000674.2:g.132673145_132673147del GRCh38
NC_000012.11:g.133249731_133249733del , CM000674.1:g.133249731_133249733del GRCh37
NC_000012.10:g.131759804_131759806del NCBI36
NG_033840.1:g.19378_19380del , LRG_789:g.19378_19380del

Transcript Alleles

HGVS Amino-acid Change
ENST00000539215.6:c.181+17_181+19del
ENST00000545015.2:n.1500+17_1500+19del
ENST00000699982.1:c.1327+17_1327+19del
ENST00000699983.1:c.1327+17_1327+19del
ENST00000699984.1:c.1327+17_1327+19del
ENST00000320574.10:c.1473+17_1473+19del MANE Select ENSP00000322570.5:n.1473+17_1473+19del
ENST00000672742.1:c.*975+17_*975+19del ENSP00000500279.1:n.*975+17_*975+19del
ENST00000320574.9:c.1473+17_1473+19del ENSP00000322570.5:n.1473+17_1473+19del
ENST00000535270.5:c.1392+17_1392+19del ENSP00000445753.1:n.1392+17_1392+19del
ENST00000535934.2:n.1348+17_1348+19del
ENST00000537064.5:c.*520+17_*520+19del ENSP00000442578.1:n.*520+17_*520+19del
ENST00000539215.5:n.181+17_181+19del
ENST00000545015.1:n.70+17_70+19del
NM_006231.3:c.1473+17_1473+19del , LRG_789t1:c.1473+17_1473+19del NP_006222.2:n.1473+17_1473+19del
XM_011534795.1:c.1473+17_1473+19del XP_011533097.1:n.1473+17_1473+19del
XM_011534796.1:c.1344+17_1344+19del XP_011533098.1:n.1344+17_1344+19del
XM_011534797.1:c.552+17_552+19del XP_011533099.1:n.552+17_552+19del
XM_011534798.1:c.135+17_135+19del XP_011533100.1:n.135+17_135+19del
XM_011534799.1:c.1473+17_1473+19del XP_011533101.1:n.1473+17_1473+19del
XM_011534800.1:c.1473+17_1473+19del XP_011533102.1:n.1473+17_1473+19del
XM_011534801.1:c.1473+17_1473+19del XP_011533103.1:n.1473+17_1473+19del
XR_941395.1:n.1682+17_1682+19del
XM_011534795.3:c.1473+17_1473+19del XP_011533097.1:n.1473+17_1473+19del
XM_011534797.3:c.552+17_552+19del XP_011533099.1:n.552+17_552+19del
XM_011534799.2:c.1473+17_1473+19del XP_011533101.1:n.1473+17_1473+19del
XR_002957338.1:n.1677+17_1677+19del
XR_002957339.1:n.1677+17_1677+19del
XR_941395.2:n.1677+17_1677+19del
NM_006231.4:c.1473+17_1473+19del MANE Select NP_006222.2:n.1473+17_1473+19del