Canonical Allele Identifier: CA1926175818

Gene: PTEN

Linked Data

• dbSNP Id: rs1860778905

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87966909_87966910insGT , CM000672.2:g.87966909_87966910insGT	GRCh38
NC_000010.10:g.89726666_89726667insGT , CM000672.1:g.89726666_89726667insGT	GRCh37
NC_000010.9:g.89716646_89716647insGT	NCBI36
NG_007466.2:g.108471_108472insGT , LRG_311:g.108471_108472insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710265.1:c.*1678_*1679insGT	ENSP00000518161.1:n.*1678_*1679insGT
ENST00000688158.2:n.3384_3385insGT
ENST00000706954.1:c.*1437_*1438insGT	ENSP00000516674.1:n.*1437_*1438insGT
ENST00000706955.1:c.*2684_*2685insGT	ENSP00000516675.1:n.*2684_*2685insGT
ENST00000688158.1:c.*2760_*2761insGT	ENSP00000509254.1:n.*2760_*2761insGT
ENST00000693560.1:c.*1437_*1438insGT	ENSP00000509861.1:n.*1437_*1438insGT
ENST00000371953.8:c.*1437_*1438insGT MANE Select	ENSP00000361021.3:n.*1437_*1438insGT
ENST00000371953.7:c.*1437_*1438insGT	ENSP00000361021.3:n.*1437_*1438insGT
NM_000314.5:c.*1437_*1438insGT	NP_000305.3:n.*1437_*1438insGT
NM_000314.6:c.*1437_*1438insGT	NP_000305.3:n.*1437_*1438insGT
NM_001304717.2:c.*1437_*1438insGT	NP_001291646.2:n.*1437_*1438insGT
NM_001304718.1:c.*1437_*1438insGT	NP_001291647.1:n.*1437_*1438insGT
XM_006717926.2:c.*1437_*1438insGT	XP_006717989.1:n.*1437_*1438insGT
XM_011539982.1:c.*1437_*1438insGT	XP_011538284.1:n.*1437_*1438insGT
XR_945791.1:n.3219_3220insGT
NM_000314.7:c.*1437_*1438insGT	NP_000305.3:n.*1437_*1438insGT
NM_001304717.5:c.*1437_*1438insGT	NP_001291646.4:n.*1437_*1438insGT
NM_001304718.2:c.*1437_*1438insGT	NP_001291647.1:n.*1437_*1438insGT
NM_000314.8:c.*1437_*1438insGT MANE Select	NP_000305.3:n.*1437_*1438insGT