Canonical Allele Identifier: CA2073001054

Gene: POLE

Linked Data

• ClinVar Variation Id: 1038132
• ClinVar RCV Id: RCV003770909
• dbSNP Id: rs1555228110
• gnomAD v4: 12-132672211-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132672211T>G , CM000674.2:g.132672211T>G	GRCh38
NC_000012.11:g.133248797T>G , CM000674.1:g.133248797T>G	GRCh37
NC_000012.10:g.131758870T>G	NCBI36
NG_033840.1:g.20314A>C , LRG_789:g.20314A>C

Transcript Alleles

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