Canonical Allele Identifier: CA645553894

Gene: PTEN

Linked Data

• COSMIC: COSM4959

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952156_87952160del , CM000672.2:g.87952156_87952160del	GRCh38
NC_000010.10:g.89711913_89711917del , CM000672.1:g.89711913_89711917del	GRCh37
NC_000010.9:g.89701893_89701897del	NCBI36
NG_007466.2:g.93718_93722del , LRG_311:g.93718_93722del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.531_535del	ENSP00000514759.2:p.Tyr177Ter
ENST00000710265.1:c.531_535del	ENSP00000518161.1:p.Tyr177Ter
ENST00000472832.3:c.531_535del	ENSP00000483066.2:p.Tyr177Ter
ENST00000688158.2:n.1266_1270del
ENST00000688922.2:c.*361_*365del	ENSP00000508742.2:n.*361_*365del
ENST00000700021.1:c.486_490del	ENSP00000514757.1:p.Tyr162Ter
ENST00000700022.1:c.493-5697_493-5693del	ENSP00000514758.1:n.493-5697_493-5693del
ENST00000700023.1:n.1689_1693del
ENST00000700024.1:n.1923_1927del
ENST00000700025.1:n.1300_1304del
ENST00000700029.1:c.365_369del
ENST00000706954.1:c.531_535del	ENSP00000516674.1:p.Tyr177Ter
ENST00000706955.1:c.*566_*570del	ENSP00000516675.1:n.*566_*570del
ENST00000686459.1:c.*117_*121del	ENSP00000508909.1:n.*117_*121del
ENST00000688158.1:c.*642_*646del	ENSP00000509254.1:n.*642_*646del
ENST00000688308.1:c.531_535del	ENSP00000508752.1:p.Tyr177Ter
ENST00000688922.1:c.452_456del
ENST00000693560.1:c.1050_1054del	ENSP00000509861.1:p.Tyr350Ter
ENST00000371953.8:c.531_535del MANE Select	ENSP00000361021.3:p.Tyr177Ter
ENST00000371953.7:c.531_535del	ENSP00000361021.3:p.Tyr177Ter
NM_000314.5:c.531_535del	NP_000305.3:p.Tyr177Ter
NM_000314.6:c.531_535del	NP_000305.3:p.Tyr177Ter
NM_001304717.2:c.1050_1054del	NP_001291646.2:p.Tyr350Ter
NM_001304718.1:c.-61_-57del	NP_001291647.1:n.-61_-57del
XM_006717926.2:c.486_490del	XP_006717989.1:p.Tyr162Ter
XM_011539981.1:c.531_535del	XP_011538283.1:p.Tyr177Ter
XM_011539982.1:c.435_439del	XP_011538284.1:p.Tyr145Ter
XR_945789.1:n.1402_1406del
XR_945790.1:n.1519_1523del
XR_945791.1:n.1205-5697_1205-5693del
NM_000314.7:c.531_535del	NP_000305.3:p.Tyr177Ter
NM_001304717.5:c.1050_1054del	NP_001291646.4:p.Tyr350Ter
NM_001304718.2:c.-61_-57del	NP_001291647.1:n.-61_-57del
NM_000314.8:c.531_535del MANE Select	NP_000305.3:p.Tyr177Ter