Canonical Allele Identifier: CA2072984168

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132639197G= , CM000674.2:g.132639197G=	GRCh38
NC_000012.11:g.133215783G= , CM000674.1:g.133215783G=	GRCh37
NC_000012.10:g.131725856G=	NCBI36
NG_033840.1:g.53328C= , LRG_789:g.53328C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006231.4:c.5480C= MANE Select	NP_006222.2:p.Ser1827=
ENST00000320574.10:c.5480C= MANE Select	ENSP00000322570.5:p.Ser1827=
NM_006231.3:c.5480C= , LRG_789t1:c.5480C=	NP_006222.2:p.Ser1827=
ENST00000320574.9:c.5480C=	ENSP00000322570.5:p.Ser1827=
ENST00000416953.3:n.3650C=
ENST00000434528.3:n.463C=
ENST00000434528.4:c.1018C=	ENSP00000500921.1:n.1018C=
ENST00000434528.5:c.1018C=	ENSP00000500921.1:n.1018C=
ENST00000535270.5:c.5399C=	ENSP00000445753.1:p.Ser1800=
ENST00000537064.5:c.*5231C=	ENSP00000442578.1:n.*5231C=
ENST00000544870.6:c.3153C=	ENSP00000479927.2:n.3153C=
ENST00000672002.1:c.3153C=	ENSP00000500233.1:n.3153C=
ENST00000672742.1:c.*5686C=	ENSP00000500279.1:n.*5686C=
ENST00000699981.1:n.3134C=
ENST00000699982.1:c.5334C=
ENST00000699983.1:c.6038C=
ENST00000699984.1:c.5334C=
XM_011534795.1:c.5480C=	XP_011533097.1:p.Ser1827=
XM_011534795.3:c.5480C=	XP_011533097.1:p.Ser1827=
XM_011534796.1:c.5351C=	XP_011533098.1:p.Ser1784=
XM_011534797.1:c.4559C=	XP_011533099.1:p.Ser1520=
XM_011534797.3:c.4559C=	XP_011533099.1:p.Ser1520=
XM_011534798.1:c.4142C=	XP_011533100.1:p.Ser1381=
XM_011534802.1:c.2468C=	XP_011533104.1:p.Ser823=
XM_011534802.3:c.2468C=	XP_011533104.1:p.Ser823=
XR_002957338.1:n.6313C=
XR_002957339.1:n.6026C=
XR_941395.2:n.5733C=