Canonical Allele Identifier: CA891841546

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952256_87952257delinsAC , CM000672.2:g.87952256_87952257delinsAC	GRCh38
NC_000010.10:g.89712013_89712014delinsAC , CM000672.1:g.89712013_89712014delinsAC	GRCh37
NC_000010.9:g.89701993_89701994delinsAC	NCBI36
NG_007466.2:g.93818_93819delinsAC , LRG_311:g.93818_93819delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.631_632delinsAC	ENSP00000514759.2:p.Cys211Thr
ENST00000710265.1:c.631_632delinsAC	ENSP00000518161.1:p.Cys211Thr
ENST00000472832.3:c.631_632delinsAC	ENSP00000483066.2:p.Cys211Thr
ENST00000688158.2:n.1366_1367delinsAC
ENST00000688922.2:c.*461_*462delinsAC	ENSP00000508742.2:n.*461_*462delinsAC
ENST00000700021.1:c.586_587delinsAC	ENSP00000514757.1:p.Cys196Thr
ENST00000700022.1:c.493-5597_493-5596delinsAC	ENSP00000514758.1:n.493-5597_493-5596delinsAC
ENST00000700023.1:n.1789_1790delinsAC
ENST00000700024.1:n.2023_2024delinsAC
ENST00000700025.1:n.1400_1401delinsAC
ENST00000700029.1:c.465_466delinsAC
ENST00000706954.1:c.631_632delinsAC	ENSP00000516674.1:p.Cys211Thr
ENST00000706955.1:c.*666_*667delinsAC	ENSP00000516675.1:n.*666_*667delinsAC
ENST00000686459.1:c.*217_*218delinsAC	ENSP00000508909.1:n.*217_*218delinsAC
ENST00000688158.1:c.*742_*743delinsAC	ENSP00000509254.1:n.*742_*743delinsAC
ENST00000688308.1:c.631_632delinsAC	ENSP00000508752.1:p.Cys211Thr
ENST00000688922.1:c.552_553delinsAC
ENST00000693560.1:c.1150_1151delinsAC	ENSP00000509861.1:p.Cys384Thr
ENST00000371953.8:c.631_632delinsAC MANE Select	ENSP00000361021.3:p.Cys211Thr
ENST00000371953.7:c.631_632delinsAC	ENSP00000361021.3:p.Cys211Thr
ENST00000472832.2:c.58_59delinsAC	ENSP00000483066.1:p.Cys20Thr
NM_000314.5:c.631_632delinsAC	NP_000305.3:p.Cys211Thr
NM_000314.6:c.631_632delinsAC	NP_000305.3:p.Cys211Thr
NM_001304717.2:c.1150_1151delinsAC	NP_001291646.2:p.Cys384Thr
NM_001304718.1:c.40_41delinsAC	NP_001291647.1:p.Cys14Thr
XM_006717926.2:c.586_587delinsAC	XP_006717989.1:p.Cys196Thr
XM_011539981.1:c.631_632delinsAC	XP_011538283.1:p.Cys211Thr
XM_011539982.1:c.535_536delinsAC	XP_011538284.1:p.Cys179Thr
XR_945791.1:n.1205-5597_1205-5596delinsAC
NM_000314.7:c.631_632delinsAC	NP_000305.3:p.Cys211Thr
NM_001304717.5:c.1150_1151delinsAC	NP_001291646.4:p.Cys384Thr
NM_001304718.2:c.40_41delinsAC	NP_001291647.1:p.Cys14Thr
NM_000314.8:c.631_632delinsAC MANE Select	NP_000305.3:p.Cys211Thr