Canonical Allele Identifier: CA891838667

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952130_87952132delinsGCT , CM000672.2:g.87952130_87952132delinsGCT	GRCh38
NC_000010.10:g.89711887_89711889delinsGCT , CM000672.1:g.89711887_89711889delinsGCT	GRCh37
NC_000010.9:g.89701867_89701869delinsGCT	NCBI36
NG_007466.2:g.93692_93694delinsGCT , LRG_311:g.93692_93694delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.505_507delinsGCT	ENSP00000514759.2:p.Pro169Ala
ENST00000710265.1:c.505_507delinsGCT	ENSP00000518161.1:p.Pro169Ala
ENST00000472832.3:c.505_507delinsGCT	ENSP00000483066.2:p.Pro169Ala
ENST00000688158.2:n.1240_1242delinsGCT
ENST00000688922.2:c.*335_*337delinsGCT	ENSP00000508742.2:n.*335_*337delinsGCT
ENST00000700021.1:c.460_462delinsGCT	ENSP00000514757.1:p.Pro154Ala
ENST00000700022.1:c.493-5723_493-5721delinsGCT	ENSP00000514758.1:n.493-5723_493-5721delinsGCT
ENST00000700023.1:n.1663_1665delinsGCT
ENST00000700024.1:n.1897_1899delinsGCT
ENST00000700025.1:n.1274_1276delinsGCT
ENST00000700029.1:c.339_341delinsGCT
ENST00000706954.1:c.505_507delinsGCT	ENSP00000516674.1:p.Pro169Ala
ENST00000706955.1:c.*540_*542delinsGCT	ENSP00000516675.1:n.*540_*542delinsGCT
ENST00000686459.1:c.*91_*93delinsGCT	ENSP00000508909.1:n.*91_*93delinsGCT
ENST00000688158.1:c.*616_*618delinsGCT	ENSP00000509254.1:n.*616_*618delinsGCT
ENST00000688308.1:c.505_507delinsGCT	ENSP00000508752.1:p.Pro169Ala
ENST00000688922.1:c.426_428delinsGCT
ENST00000693560.1:c.1024_1026delinsGCT	ENSP00000509861.1:p.Pro342Ala
ENST00000371953.8:c.505_507delinsGCT MANE Select	ENSP00000361021.3:p.Pro169Ala
ENST00000371953.7:c.505_507delinsGCT	ENSP00000361021.3:p.Pro169Ala
NM_000314.5:c.505_507delinsGCT	NP_000305.3:p.Pro169Ala
NM_000314.6:c.505_507delinsGCT	NP_000305.3:p.Pro169Ala
NM_001304717.2:c.1024_1026delinsGCT	NP_001291646.2:p.Pro342Ala
NM_001304718.1:c.-87_-85delinsGCT	NP_001291647.1:n.-87_-85delinsGCT
XM_006717926.2:c.460_462delinsGCT	XP_006717989.1:p.Pro154Ala
XM_011539981.1:c.505_507delinsGCT	XP_011538283.1:p.Pro169Ala
XM_011539982.1:c.409_411delinsGCT	XP_011538284.1:p.Pro137Ala
XR_945789.1:n.1376_1378delinsGCT
XR_945790.1:n.1493_1495delinsGCT
XR_945791.1:n.1205-5723_1205-5721delinsGCT
NM_000314.7:c.505_507delinsGCT	NP_000305.3:p.Pro169Ala
NM_001304717.5:c.1024_1026delinsGCT	NP_001291646.4:p.Pro342Ala
NM_001304718.2:c.-87_-85delinsGCT	NP_001291647.1:n.-87_-85delinsGCT
NM_000314.8:c.505_507delinsGCT MANE Select	NP_000305.3:p.Pro169Ala