Canonical Allele Identifier: CA387358842

Gene: POLE

Linked Data

• gnomAD v4: 12-132673270-G-T
• MyVariant Identifiers: chr12:g.133249856G>T (hg19) ; chr12:g.132673270G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132673270G>T , CM000674.2:g.132673270G>T	GRCh38
NC_000012.11:g.133249856G>T , CM000674.1:g.133249856G>T	GRCh37
NC_000012.10:g.131759929G>T	NCBI36
NG_033840.1:g.19255C>A , LRG_789:g.19255C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539215.6:c.75C>A
ENST00000545015.2:n.1394C>A
ENST00000699982.1:c.1221C>A
ENST00000699983.1:c.1221C>A
ENST00000699984.1:c.1221C>A
ENST00000320574.10:c.1367C>A MANE Select	ENSP00000322570.5:p.Ala456Asp
ENST00000672742.1:c.*869C>A	ENSP00000500279.1:n.*869C>A
ENST00000320574.9:c.1367C>A	ENSP00000322570.5:p.Ala456Asp
ENST00000535270.5:c.1286C>A	ENSP00000445753.1:p.Ala429Asp
ENST00000535934.2:n.1242C>A
ENST00000537064.5:c.*414C>A	ENSP00000442578.1:n.*414C>A
ENST00000539215.5:n.75C>A
NM_006231.3:c.1367C>A , LRG_789t1:c.1367C>A	NP_006222.2:p.Ala456Asp
XM_011534795.1:c.1367C>A	XP_011533097.1:p.Ala456Asp
XM_011534796.1:c.1238C>A	XP_011533098.1:p.Ala413Asp
XM_011534797.1:c.446C>A	XP_011533099.1:p.Ala149Asp
XM_011534798.1:c.29C>A	XP_011533100.1:p.Ala10Asp
XM_011534799.1:c.1367C>A	XP_011533101.1:p.Ala456Asp
XM_011534800.1:c.1367C>A	XP_011533102.1:p.Ala456Asp
XM_011534801.1:c.1367C>A	XP_011533103.1:p.Ala456Asp
XR_941395.1:n.1576C>A
XM_011534795.3:c.1367C>A	XP_011533097.1:p.Ala456Asp
XM_011534797.3:c.446C>A	XP_011533099.1:p.Ala149Asp
XM_011534799.2:c.1367C>A	XP_011533101.1:p.Ala456Asp
XR_002957338.1:n.1571C>A
XR_002957339.1:n.1571C>A
XR_941395.2:n.1571C>A
NM_006231.4:c.1367C>A MANE Select	NP_006222.2:p.Ala456Asp