Canonical Allele Identifier: CA2073000901

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132671946A= , CM000674.2:g.132671946A=	GRCh38
NC_000012.11:g.133248532A= , CM000674.1:g.133248532A=	GRCh37
NC_000012.10:g.131758605A=	NCBI36
NG_033840.1:g.20579T= , LRG_789:g.20579T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.549+269T=
ENST00000699982.1:c.1648+269T=
ENST00000699983.1:c.1648+269T=
ENST00000699984.1:c.1648+269T=
ENST00000320574.10:c.1794+269T= MANE Select	ENSP00000322570.5:n.1794+269T=
ENST00000672742.1:c.*1296+269T=	ENSP00000500279.1:n.*1296+269T=
ENST00000320574.9:c.1794+269T=	ENSP00000322570.5:n.1794+269T=
ENST00000535270.5:c.1713+269T=	ENSP00000445753.1:n.1713+269T=
ENST00000537064.5:c.*841+269T=	ENSP00000442578.1:n.*841+269T=
NM_006231.3:c.1794+269T= , LRG_789t1:c.1794+269T=	NP_006222.2:n.1794+269T=
XM_011534795.1:c.1794+269T=	XP_011533097.1:n.1794+269T=
XM_011534796.1:c.1665+269T=	XP_011533098.1:n.1665+269T=
XM_011534797.1:c.873+269T=	XP_011533099.1:n.873+269T=
XM_011534798.1:c.456+269T=	XP_011533100.1:n.456+269T=
XM_011534799.1:c.1794+269T=	XP_011533101.1:n.1794+269T=
XM_011534800.1:c.1794+269T=	XP_011533102.1:n.1794+269T=
XM_011534801.1:c.1794+269T=	XP_011533103.1:n.1794+269T=
XR_941395.1:n.2003+269T=
XM_011534795.3:c.1794+269T=	XP_011533097.1:n.1794+269T=
XM_011534797.3:c.873+269T=	XP_011533099.1:n.873+269T=
XM_011534799.2:c.1794+269T=	XP_011533101.1:n.1794+269T=
XR_002957338.1:n.1998+269T=
XR_002957339.1:n.1998+269T=
XR_941395.2:n.1998+269T=
NM_006231.4:c.1794+269T= MANE Select	NP_006222.2:n.1794+269T=