Canonical Allele Identifier: CA377784554

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894085G>C , CM000672.2:g.87894085G>C	GRCh38
NC_000010.10:g.89653842G>C , CM000672.1:g.89653842G>C	GRCh37
NC_000010.9:g.89643822G>C	NCBI36
NG_007466.2:g.35647G>C , LRG_311:g.35647G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.140G>C MANE Select	NP_000305.3:p.Arg47Thr
ENST00000371953.8:c.140G>C MANE Select	ENSP00000361021.3:p.Arg47Thr
NM_000314.5:c.140G>C	NP_000305.3:p.Arg47Thr
NM_000314.6:c.140G>C	NP_000305.3:p.Arg47Thr
NM_000314.7:c.140G>C	NP_000305.3:p.Arg47Thr
NM_001304717.2:c.659G>C	NP_001291646.2:p.Arg220Thr
NM_001304717.5:c.659G>C	NP_001291646.4:p.Arg220Thr
NM_001304718.1:c.-566G>C	NP_001291647.1:n.-566G>C
NM_001304718.2:c.-566G>C	NP_001291647.1:n.-566G>C
ENST00000371953.7:c.140G>C	ENSP00000361021.3:p.Arg47Thr
ENST00000462694.1:n.142G>C
ENST00000472832.3:c.140G>C	ENSP00000483066.2:p.Arg47Thr
ENST00000610634.1:c.38G>C	ENSP00000477517.1:p.Arg13Thr
ENST00000686459.1:c.140G>C	ENSP00000508909.1:p.Arg47Thr
ENST00000688158.1:c.*275+13647G>C	ENSP00000509254.1:n.*275+13647G>C
ENST00000688158.2:n.899+13647G>C
ENST00000688308.1:c.140G>C	ENSP00000508752.1:p.Arg47Thr
ENST00000688922.1:c.9G>C
ENST00000688922.2:c.140G>C	ENSP00000508742.2:p.Arg47Thr
ENST00000693560.1:c.659G>C	ENSP00000509861.1:p.Arg220Thr
ENST00000700021.1:c.140G>C	ENSP00000514757.1:p.Arg47Thr
ENST00000700022.1:c.140G>C	ENSP00000514758.1:p.Arg47Thr
ENST00000700029.2:c.140G>C	ENSP00000514759.2:p.Arg47Thr
ENST00000706954.1:c.140G>C	ENSP00000516674.1:p.Arg47Thr
ENST00000706955.1:c.*175G>C	ENSP00000516675.1:n.*175G>C
ENST00000710265.1:c.140G>C	ENSP00000518161.1:p.Arg47Thr
XM_006717926.2:c.140G>C	XP_006717989.1:p.Arg47Thr
XM_011539981.1:c.140G>C	XP_011538283.1:p.Arg47Thr
XM_011539982.1:c.68+13647G>C	XP_011538284.1:n.68+13647G>C
XR_945789.1:n.852G>C
XR_945790.1:n.852G>C
XR_945791.1:n.852G>C