Canonical Allele Identifier: CA387356202

Gene: POLE

Linked Data

• MyVariant Identifiers: chr12:g.133248801C>A (hg19) ; chr12:g.132672215C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132672215C>A , CM000674.2:g.132672215C>A	GRCh38
NC_000012.11:g.133248801C>A , CM000674.1:g.133248801C>A	GRCh37
NC_000012.10:g.131758874C>A	NCBI36
NG_033840.1:g.20310G>T , LRG_789:g.20310G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.549G>T
ENST00000699982.1:c.1648G>T
ENST00000699983.1:c.1648G>T
ENST00000699984.1:c.1648G>T
ENST00000320574.10:c.1794G>T MANE Select	ENSP00000322570.5:p.Glu598Asp
ENST00000672742.1:c.*1296G>T	ENSP00000500279.1:n.*1296G>T
ENST00000320574.9:c.1794G>T	ENSP00000322570.5:p.Glu598Asp
ENST00000535270.5:c.1713G>T	ENSP00000445753.1:p.Glu571Asp
ENST00000537064.5:c.*841G>T	ENSP00000442578.1:n.*841G>T
NM_006231.3:c.1794G>T , LRG_789t1:c.1794G>T	NP_006222.2:p.Glu598Asp
XM_011534795.1:c.1794G>T	XP_011533097.1:p.Glu598Asp
XM_011534796.1:c.1665G>T	XP_011533098.1:p.Glu555Asp
XM_011534797.1:c.873G>T	XP_011533099.1:p.Glu291Asp
XM_011534798.1:c.456G>T	XP_011533100.1:p.Glu152Asp
XM_011534799.1:c.1794G>T	XP_011533101.1:p.Glu598Asp
XM_011534800.1:c.1794G>T	XP_011533102.1:p.Glu598Asp
XM_011534801.1:c.1794G>T	XP_011533103.1:p.Glu598Asp
XR_941395.1:n.2003G>T
XM_011534795.3:c.1794G>T	XP_011533097.1:p.Glu598Asp
XM_011534797.3:c.873G>T	XP_011533099.1:p.Glu291Asp
XM_011534799.2:c.1794G>T	XP_011533101.1:p.Glu598Asp
XR_002957338.1:n.1998G>T
XR_002957339.1:n.1998G>T
XR_941395.2:n.1998G>T
NM_006231.4:c.1794G>T MANE Select	NP_006222.2:p.Glu598Asp