Canonical Allele Identifier: CA891837049

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965311_87965313delinsTGT , CM000672.2:g.87965311_87965313delinsTGT	GRCh38
NC_000010.10:g.89725068_89725070delinsTGT , CM000672.1:g.89725068_89725070delinsTGT	GRCh37
NC_000010.9:g.89715048_89715050delinsTGT	NCBI36
NG_007466.2:g.106873_106875delinsTGT , LRG_311:g.106873_106875delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1144_1146delinsTGT	ENSP00000514759.2:p.Val382Cys
ENST00000710265.1:c.*80_*82delinsTGT	ENSP00000518161.1:n.*80_*82delinsTGT
ENST00000688158.2:n.1786_1788delinsTGT
ENST00000688922.2:c.*881_*883delinsTGT	ENSP00000508742.2:n.*881_*883delinsTGT
ENST00000700021.1:c.1006_1008delinsTGT	ENSP00000514757.1:p.Val336Cys
ENST00000700022.1:c.*390_*392delinsTGT	ENSP00000514758.1:n.*390_*392delinsTGT
ENST00000700023.1:n.2209_2211delinsTGT
ENST00000700024.1:n.2443_2445delinsTGT
ENST00000706954.1:c.1051_1053delinsTGT	ENSP00000516674.1:p.Val351Cys
ENST00000706955.1:c.*1086_*1088delinsTGT	ENSP00000516675.1:n.*1086_*1088delinsTGT
ENST00000686459.1:c.*637_*639delinsTGT	ENSP00000508909.1:n.*637_*639delinsTGT
ENST00000688158.1:c.*1162_*1164delinsTGT	ENSP00000509254.1:n.*1162_*1164delinsTGT
ENST00000688308.1:c.1051_1053delinsTGT	ENSP00000508752.1:p.Val351Cys
ENST00000688922.1:c.972_974delinsTGT
ENST00000693560.1:c.1570_1572delinsTGT	ENSP00000509861.1:p.Val524Cys
ENST00000371953.8:c.1051_1053delinsTGT MANE Select	ENSP00000361021.3:p.Val351Cys
ENST00000371953.7:c.1051_1053delinsTGT	ENSP00000361021.3:p.Val351Cys
NM_000314.5:c.1051_1053delinsTGT	NP_000305.3:p.Val351Cys
NM_000314.6:c.1051_1053delinsTGT	NP_000305.3:p.Val351Cys
NM_001304717.2:c.1570_1572delinsTGT	NP_001291646.2:p.Val524Cys
NM_001304718.1:c.460_462delinsTGT	NP_001291647.1:p.Val154Cys
XM_006717926.2:c.1006_1008delinsTGT	XP_006717989.1:p.Val336Cys
XM_011539982.1:c.955_957delinsTGT	XP_011538284.1:p.Val319Cys
XR_945791.1:n.1621_1623delinsTGT
NM_000314.7:c.1051_1053delinsTGT	NP_000305.3:p.Val351Cys
NM_001304717.5:c.1570_1572delinsTGT	NP_001291646.4:p.Val524Cys
NM_001304718.2:c.460_462delinsTGT	NP_001291647.1:p.Val154Cys
NM_000314.8:c.1051_1053delinsTGT MANE Select	NP_000305.3:p.Val351Cys