Canonical Allele Identifier: CA2695200889

Gene: PTEN

Linked Data

• ClinVar Variation Id: 2674299
• ClinVar RCV Id: RCV003452495

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960840_87960975del , CM000672.2:g.87960840_87960975del	GRCh38
NC_000010.10:g.89720597_89720732del , CM000672.1:g.89720597_89720732del	GRCh37
NC_000010.9:g.89710577_89710712del	NCBI36
NG_007466.2:g.102402_102537del , LRG_311:g.102402_102537del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-54_976del
ENST00000710265.1:c.802-54_883del
ENST00000472832.3:c.802-54_883del
ENST00000688158.2:n.1537-54_1618del
ENST00000688922.2:c.*632-54_*713del
ENST00000700021.1:c.757-54_838del
ENST00000700022.1:c.*141-54_*222del
ENST00000700023.1:n.1960-54_2041del
ENST00000700024.1:n.2194-54_2275del
ENST00000700025.1:n.1571-54_1652del
ENST00000700026.1:n.439-54_520del
ENST00000706954.1:c.802-54_883del
ENST00000706955.1:c.*837-54_*918del
ENST00000686459.1:c.*388-54_*469del
ENST00000688158.1:c.*913-54_*994del
ENST00000688308.1:c.802-54_883del
ENST00000688922.1:c.723-54_804del
ENST00000693560.1:c.1321-54_1402del
ENST00000371953.8:c.802-54_883del
ENST00000371953.7:c.802-54_883del
ENST00000472832.2:c.229-54_310del
NM_000314.5:c.802-54_883del
NM_000314.6:c.802-54_883del
NM_001304717.2:c.1321-54_1402del
NM_001304718.1:c.211-54_292del
XM_006717926.2:c.757-54_838del
XM_011539981.1:c.802-54_883del
XM_011539982.1:c.706-54_787del
XR_945791.1:n.1372-54_1453del
NM_000314.7:c.802-54_883del
NM_001304717.5:c.1321-54_1402del
NM_001304718.2:c.211-54_292del
NM_000314.8:c.802-54_883del