Canonical Allele Identifier: CA658798008

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132624894_132624897del , CM000674.2:g.132624894_132624897del	GRCh38
NC_000012.11:g.133201480_133201483del , CM000674.1:g.133201480_133201483del	GRCh37
NC_000012.10:g.131711553_131711556del	NCBI36
NG_033840.1:g.67631_67634del , LRG_789:g.67631_67634del

Transcript Alleles

HGVS	Amino-acid Change
NM_006231.4:c.6747+11_6747+14del MANE Select	NP_006222.2:n.6747+11_6747+14del
ENST00000320574.10:c.6747+11_6747+14del MANE Select	ENSP00000322570.5:n.6747+11_6747+14del
NM_006231.3:c.6747+11_6747+14del , LRG_789t1:c.6747+11_6747+14del	NP_006222.2:n.6747+11_6747+14del
ENST00000320574.9:c.6747+11_6747+14del	ENSP00000322570.5:n.6747+11_6747+14del
ENST00000434528.4:c.2285+11_2285+14del	ENSP00000500921.1:n.2285+11_2285+14del
ENST00000434528.5:c.2285+11_2285+14del	ENSP00000500921.1:n.2285+11_2285+14del
ENST00000534922.5:n.1321_1324del
ENST00000535270.5:c.6666+11_6666+14del	ENSP00000445753.1:n.6666+11_6666+14del
ENST00000537064.5:c.*6498+11_*6498+14del	ENSP00000442578.1:n.*6498+11_*6498+14del
ENST00000541627.2:n.1047+11_1047+14del
ENST00000544692.5:n.2116+11_2116+14del
ENST00000544870.6:c.4400+11_4400+14del	ENSP00000479927.2:n.4400+11_4400+14del
ENST00000672002.1:c.4420+11_4420+14del	ENSP00000500233.1:n.4420+11_4420+14del
ENST00000672742.1:c.*6953+11_*6953+14del	ENSP00000500279.1:n.*6953+11_*6953+14del
ENST00000699981.1:n.4401+11_4401+14del
ENST00000699982.1:c.6601+11_6601+14del
ENST00000699983.1:c.7305+11_7305+14del
ENST00000699984.1:c.6533+11_6533+14del
XR_002957339.1:n.7639+11_7639+14del