Canonical Allele Identifier: CA2695200866

Gene: PTEN

Linked Data

• ClinVar Variation Id: 2674397
• ClinVar RCV Id: RCV003452593

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957853_87957860del , CM000672.2:g.87957853_87957860del	GRCh38
NC_000010.10:g.89717610_89717617del , CM000672.1:g.89717610_89717617del	GRCh37
NC_000010.9:g.89707590_89707597del	NCBI36
NG_007466.2:g.99415_99422del , LRG_311:g.99415_99422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.635_642del
ENST00000710265.1:c.635_642del
ENST00000472832.3:c.635_642del
ENST00000688158.2:n.1370_1377del
ENST00000688922.2:c.*465_*472del
ENST00000700021.1:c.590_597del
ENST00000700022.1:c.493_500del
ENST00000700023.1:n.1793_1800del
ENST00000700024.1:n.2027_2034del
ENST00000700025.1:n.1404_1411del
ENST00000700026.1:n.272_279del
ENST00000700029.1:c.469_476del
ENST00000706954.1:c.635_642del
ENST00000706955.1:c.*670_*677del
ENST00000686459.1:c.*221_*228del
ENST00000688158.1:c.*746_*753del
ENST00000688308.1:c.635_642del
ENST00000688922.1:c.556_563del
ENST00000693560.1:c.1154_1161del
ENST00000371953.8:c.635_642del
ENST00000371953.7:c.635_642del
ENST00000472832.2:c.62_69del
NM_000314.5:c.635_642del
NM_000314.6:c.635_642del
NM_001304717.2:c.1154_1161del
NM_001304718.1:c.44_51del
XM_006717926.2:c.590_597del
XM_011539981.1:c.635_642del
XM_011539982.1:c.539_546del
XR_945791.1:n.1205_1212del
NM_000314.7:c.635_642del
NM_001304717.5:c.1154_1161del
NM_001304718.2:c.44_51del
NM_000314.8:c.635_642del