Canonical Allele Identifier: CA6893308
Gene: POLE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132659279_132659304del , CM000674.2:g.132659279_132659304del GRCh38
NC_000012.11:g.133235865_133235890del , CM000674.1:g.133235865_133235890del GRCh37
NC_000012.10:g.131745938_131745963del NCBI36
NG_033840.1:g.33242_33267del , LRG_789:g.33242_33267del

Transcript Alleles

HGVS Amino-acid Change
ENST00000544870.6:c.896+12_896+37del
ENST00000699982.1:c.3129+12_3129+37del
ENST00000699983.1:c.3129+12_3129+37del
ENST00000699984.1:c.3129+12_3129+37del
ENST00000320574.10:c.3275+12_3275+37del
ENST00000672002.1:c.896+12_896+37del
ENST00000672742.1:c.*2777+12_*2777+37del
ENST00000320574.9:c.3275+12_3275+37del
ENST00000535270.5:c.3194+12_3194+37del
ENST00000536445.5:n.1619+12_1619+37del
ENST00000537064.5:c.*2322+12_*2322+37del
NM_006231.3:c.3275+12_3275+37del , LRG_789t1:c.3275+12_3275+37del
XM_011534795.1:c.3275+12_3275+37del
XM_011534796.1:c.3146+12_3146+37del
XM_011534797.1:c.2354+12_2354+37del
XM_011534798.1:c.1937+12_1937+37del
XM_011534799.1:c.3275+12_3275+37del
XM_011534800.1:c.3275+12_3275+37del
XM_011534801.1:c.3275+12_3275+37del
XM_011534802.1:c.263+12_263+37del
XR_941395.1:n.3484+12_3484+37del
XM_011534795.3:c.3275+12_3275+37del
XM_011534797.3:c.2354+12_2354+37del
XM_011534799.2:c.3275+12_3275+37del
XM_011534802.3:c.263+12_263+37del
XR_002957338.1:n.3479+12_3479+37del
XR_002957339.1:n.3479+12_3479+37del
XR_941395.2:n.3479+12_3479+37del
NM_006231.4:c.3275+12_3275+37del