Canonical Allele Identifier: CA891837508

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965359_87965361delinsGTT , CM000672.2:g.87965359_87965361delinsGTT	GRCh38
NC_000010.10:g.89725116_89725118delinsGTT , CM000672.1:g.89725116_89725118delinsGTT	GRCh37
NC_000010.9:g.89715096_89715098delinsGTT	NCBI36
NG_007466.2:g.106921_106923delinsGTT , LRG_311:g.106921_106923delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1192_1194delinsGTT	ENSP00000514759.2:p.Pro398Val
ENST00000710265.1:c.*128_*130delinsGTT	ENSP00000518161.1:n.*128_*130delinsGTT
ENST00000688158.2:n.1834_1836delinsGTT
ENST00000688922.2:c.*929_*931delinsGTT	ENSP00000508742.2:n.*929_*931delinsGTT
ENST00000700021.1:c.1054_1056delinsGTT	ENSP00000514757.1:p.Pro352Val
ENST00000700022.1:c.*438_*440delinsGTT	ENSP00000514758.1:n.*438_*440delinsGTT
ENST00000700023.1:n.2257_2259delinsGTT
ENST00000700024.1:n.2491_2493delinsGTT
ENST00000706954.1:c.1099_1101delinsGTT	ENSP00000516674.1:p.Pro367Val
ENST00000706955.1:c.*1134_*1136delinsGTT	ENSP00000516675.1:n.*1134_*1136delinsGTT
ENST00000686459.1:c.*685_*687delinsGTT	ENSP00000508909.1:n.*685_*687delinsGTT
ENST00000688158.1:c.*1210_*1212delinsGTT	ENSP00000509254.1:n.*1210_*1212delinsGTT
ENST00000688308.1:c.1099_1101delinsGTT	ENSP00000508752.1:p.Pro367Val
ENST00000688922.1:c.1020_1022delinsGTT
ENST00000693560.1:c.1618_1620delinsGTT	ENSP00000509861.1:p.Pro540Val
ENST00000371953.8:c.1099_1101delinsGTT MANE Select	ENSP00000361021.3:p.Pro367Val
ENST00000371953.7:c.1099_1101delinsGTT	ENSP00000361021.3:p.Pro367Val
NM_000314.5:c.1099_1101delinsGTT	NP_000305.3:p.Pro367Val
NM_000314.6:c.1099_1101delinsGTT	NP_000305.3:p.Pro367Val
NM_001304717.2:c.1618_1620delinsGTT	NP_001291646.2:p.Pro540Val
NM_001304718.1:c.508_510delinsGTT	NP_001291647.1:p.Pro170Val
XM_006717926.2:c.1054_1056delinsGTT	XP_006717989.1:p.Pro352Val
XM_011539982.1:c.1003_1005delinsGTT	XP_011538284.1:p.Pro335Val
XR_945791.1:n.1669_1671delinsGTT
NM_000314.7:c.1099_1101delinsGTT	NP_000305.3:p.Pro367Val
NM_001304717.5:c.1618_1620delinsGTT	NP_001291646.4:p.Pro540Val
NM_001304718.2:c.508_510delinsGTT	NP_001291647.1:p.Pro170Val
NM_000314.8:c.1099_1101delinsGTT MANE Select	NP_000305.3:p.Pro367Val