Canonical Allele Identifier: CA645554080

Gene: PTEN

Linked Data

• COSMIC: COSM921137

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960900_87960904del , CM000672.2:g.87960900_87960904del	GRCh38
NC_000010.10:g.89720657_89720661del , CM000672.1:g.89720657_89720661del	GRCh37
NC_000010.9:g.89710637_89710641del	NCBI36
NG_007466.2:g.102462_102466del , LRG_311:g.102462_102466del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.901_905del	ENSP00000514759.2:p.Met301SerfsTer26
ENST00000710265.1:c.808_812del	ENSP00000518161.1:p.Met270SerfsTer26
ENST00000472832.3:c.808_812del	ENSP00000483066.2:p.Met270SerfsTer26
ENST00000688158.2:n.1543_1547del
ENST00000688922.2:c.*638_*642del	ENSP00000508742.2:n.*638_*642del
ENST00000700021.1:c.763_767del	ENSP00000514757.1:p.Met255SerfsTer26
ENST00000700022.1:c.*147_*151del	ENSP00000514758.1:n.*147_*151del
ENST00000700023.1:n.1966_1970del
ENST00000700024.1:n.2200_2204del
ENST00000700025.1:n.1577_1581del
ENST00000700026.1:n.445_449del
ENST00000700029.1:c.735_739del
ENST00000706954.1:c.808_812del	ENSP00000516674.1:p.Met270SerfsTer26
ENST00000706955.1:c.*843_*847del	ENSP00000516675.1:n.*843_*847del
ENST00000686459.1:c.*394_*398del	ENSP00000508909.1:n.*394_*398del
ENST00000688158.1:c.*919_*923del	ENSP00000509254.1:n.*919_*923del
ENST00000688308.1:c.808_812del	ENSP00000508752.1:p.Met270SerfsTer26
ENST00000688922.1:c.729_733del
ENST00000693560.1:c.1327_1331del	ENSP00000509861.1:p.Met443SerfsTer26
ENST00000371953.8:c.808_812del MANE Select	ENSP00000361021.3:p.Met270SerfsTer26
ENST00000371953.7:c.808_812del	ENSP00000361021.3:p.Met270SerfsTer26
ENST00000472832.2:c.235_239del	ENSP00000483066.1:p.Met79SerfsTer26
NM_000314.5:c.808_812del	NP_000305.3:p.Met270SerfsTer26
NM_000314.6:c.808_812del	NP_000305.3:p.Met270SerfsTer26
NM_001304717.2:c.1327_1331del	NP_001291646.2:p.Met443SerfsTer26
NM_001304718.1:c.217_221del	NP_001291647.1:p.Met73SerfsTer26
XM_006717926.2:c.763_767del	XP_006717989.1:p.Met255SerfsTer26
XM_011539981.1:c.808_812del	XP_011538283.1:p.Met270SerfsTer26
XM_011539982.1:c.712_716del	XP_011538284.1:p.Met238SerfsTer26
XR_945791.1:n.1378_1382del
NM_000314.7:c.808_812del	NP_000305.3:p.Met270SerfsTer26
NM_001304717.5:c.1327_1331del	NP_001291646.4:p.Met443SerfsTer26
NM_001304718.2:c.217_221del	NP_001291647.1:p.Met73SerfsTer26
NM_000314.8:c.808_812del MANE Select	NP_000305.3:p.Met270SerfsTer26