Canonical Allele Identifier: CA645553890

Gene: PTEN

Linked Data

• COSMIC: COSM4938

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952140_87952158del , CM000672.2:g.87952140_87952158del	GRCh38
NC_000010.10:g.89711897_89711915del , CM000672.1:g.89711897_89711915del	GRCh37
NC_000010.9:g.89701877_89701895del	NCBI36
NG_007466.2:g.93702_93720del , LRG_311:g.93702_93720del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.515_533del	ENSP00000514759.2:p.Arg172IlefsTer5
ENST00000710265.1:c.515_533del	ENSP00000518161.1:p.Arg172IlefsTer5
ENST00000472832.3:c.515_533del	ENSP00000483066.2:p.Arg172IlefsTer5
ENST00000688158.2:n.1250_1268del
ENST00000688922.2:c.*345_*363del	ENSP00000508742.2:n.*345_*363del
ENST00000700021.1:c.470_488del	ENSP00000514757.1:p.Arg157IlefsTer5
ENST00000700022.1:c.493-5713_493-5695del	ENSP00000514758.1:n.493-5713_493-5695del
ENST00000700023.1:n.1673_1691del
ENST00000700024.1:n.1907_1925del
ENST00000700025.1:n.1284_1302del
ENST00000700029.1:c.349_367del
ENST00000706954.1:c.515_533del	ENSP00000516674.1:p.Arg172IlefsTer5
ENST00000706955.1:c.*550_*568del	ENSP00000516675.1:n.*550_*568del
ENST00000686459.1:c.*101_*119del	ENSP00000508909.1:n.*101_*119del
ENST00000688158.1:c.*626_*644del	ENSP00000509254.1:n.*626_*644del
ENST00000688308.1:c.515_533del	ENSP00000508752.1:p.Arg172IlefsTer5
ENST00000688922.1:c.436_454del
ENST00000693560.1:c.1034_1052del	ENSP00000509861.1:p.Arg345IlefsTer5
ENST00000371953.8:c.515_533del MANE Select	ENSP00000361021.3:p.Arg172IlefsTer5
ENST00000371953.7:c.515_533del	ENSP00000361021.3:p.Arg172IlefsTer5
NM_000314.5:c.515_533del	NP_000305.3:p.Arg172IlefsTer5
NM_000314.6:c.515_533del	NP_000305.3:p.Arg172IlefsTer5
NM_001304717.2:c.1034_1052del	NP_001291646.2:p.Arg345IlefsTer5
NM_001304718.1:c.-77_-59del	NP_001291647.1:n.-77_-59del
XM_006717926.2:c.470_488del	XP_006717989.1:p.Arg157IlefsTer5
XM_011539981.1:c.515_533del	XP_011538283.1:p.Arg172IlefsTer5
XM_011539982.1:c.419_437del	XP_011538284.1:p.Arg140IlefsTer5
XR_945789.1:n.1386_1404del
XR_945790.1:n.1503_1521del
XR_945791.1:n.1205-5713_1205-5695del
NM_000314.7:c.515_533del	NP_000305.3:p.Arg172IlefsTer5
NM_001304717.5:c.1034_1052del	NP_001291646.4:p.Arg345IlefsTer5
NM_001304718.2:c.-77_-59del	NP_001291647.1:n.-77_-59del
NM_000314.8:c.515_533del MANE Select	NP_000305.3:p.Arg172IlefsTer5