Canonical Allele Identifier: CA645553879

Gene: PTEN

Linked Data

• COSMIC: COSM5873

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952119_87952260del , CM000672.2:g.87952119_87952260del	GRCh38
NC_000010.10:g.89711876_89712017del , CM000672.1:g.89711876_89712017del	GRCh37
NC_000010.9:g.89701856_89701997del	NCBI36
NG_007466.2:g.93681_93822del , LRG_311:g.93681_93822del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.494_634+1del
ENST00000710265.1:c.494_634+1del
ENST00000472832.3:c.494_634+1del
ENST00000688158.2:n.1229_1369+1del
ENST00000688922.2:c.*324_*464+1del
ENST00000700021.1:c.449_589+1del
ENST00000700022.1:c.493-5734_493-5593del	ENSP00000514758.1:n.493-5734_493-5593del
ENST00000700023.1:n.1652_1792+1del
ENST00000700024.1:n.1886_2026+1del
ENST00000700025.1:n.1263_1403+1del
ENST00000700029.1:c.328_468+1del
ENST00000706954.1:c.494_634+1del
ENST00000706955.1:c.*529_*669+1del
ENST00000686459.1:c.*80_*220+1del
ENST00000688158.1:c.*605_*745+1del
ENST00000688308.1:c.494_634+1del
ENST00000688922.1:c.415_555+1del
ENST00000693560.1:c.1013_1153+1del
ENST00000371953.8:c.494_634+1del
ENST00000371953.7:c.494_634+1del
NM_000314.5:c.494_634+1del
NM_000314.6:c.494_634+1del
NM_001304717.2:c.1013_1153+1del
NM_001304718.1:c.-98_43+1del
XM_006717926.2:c.449_589+1del
XM_011539981.1:c.494_634+1del
XM_011539982.1:c.398_538+1del
XR_945791.1:n.1205-5734_1205-5593del
NM_000314.7:c.494_634+1del
NM_001304717.5:c.1013_1153+1del
NM_001304718.2:c.-98_43+1del
NM_000314.8:c.494_634+1del