Canonical Allele Identifier: CA2073003432

Gene: POLE

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132676594A= , CM000674.2:g.132676594A=	GRCh38
NC_000012.11:g.133253180A= , CM000674.1:g.133253180A=	GRCh37
NC_000012.10:g.131763253A=	NCBI36
NG_033840.1:g.15931T= , LRG_789:g.15931T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006231.4:c.861T= MANE Select	NP_006222.2:p.Asp287=
ENST00000320574.10:c.861T= MANE Select	ENSP00000322570.5:p.Asp287=
NM_006231.3:c.861T= , LRG_789t1:c.861T=	NP_006222.2:p.Asp287=
ENST00000320574.9:c.861T=	ENSP00000322570.5:p.Asp287=
ENST00000535270.5:c.780T=	ENSP00000445753.1:p.Asp260=
ENST00000537064.5:c.861T=	ENSP00000442578.1:p.Asp287=
ENST00000545015.2:n.888T=
ENST00000672742.1:c.*355T=	ENSP00000500279.1:n.*355T=
ENST00000699982.1:c.707T=
ENST00000699983.1:c.707T=
ENST00000699984.1:c.707T=
XM_011534795.1:c.861T=	XP_011533097.1:p.Asp287=
XM_011534795.3:c.861T=	XP_011533097.1:p.Asp287=
XM_011534796.1:c.732T=	XP_011533098.1:p.Asp244=
XM_011534797.1:c.-41T=	XP_011533099.1:n.-41T=
XM_011534797.3:c.-41T=	XP_011533099.1:n.-41T=
XM_011534799.1:c.861T=	XP_011533101.1:p.Asp287=
XM_011534799.2:c.861T=	XP_011533101.1:p.Asp287=
XM_011534800.1:c.861T=	XP_011533102.1:p.Asp287=
XM_011534801.1:c.861T=	XP_011533103.1:p.Asp287=
XR_002957338.1:n.1065T=
XR_002957339.1:n.1065T=
XR_941395.1:n.1070T=
XR_941395.2:n.1065T=