Canonical Allele Identifier: CA891837469

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965354_87965355delinsAT , CM000672.2:g.87965354_87965355delinsAT	GRCh38
NC_000010.10:g.89725111_89725112delinsAT , CM000672.1:g.89725111_89725112delinsAT	GRCh37
NC_000010.9:g.89715091_89715092delinsAT	NCBI36
NG_007466.2:g.106916_106917delinsAT , LRG_311:g.106916_106917delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1187_1188delinsAT	ENSP00000514759.2:p.Val396Asp
ENST00000710265.1:c.*123_*124delinsAT	ENSP00000518161.1:n.*123_*124delinsAT
ENST00000688158.2:n.1829_1830delinsAT
ENST00000688922.2:c.*924_*925delinsAT	ENSP00000508742.2:n.*924_*925delinsAT
ENST00000700021.1:c.1049_1050delinsAT	ENSP00000514757.1:p.Val350Asp
ENST00000700022.1:c.*433_*434delinsAT	ENSP00000514758.1:n.*433_*434delinsAT
ENST00000700023.1:n.2252_2253delinsAT
ENST00000700024.1:n.2486_2487delinsAT
ENST00000706954.1:c.1094_1095delinsAT	ENSP00000516674.1:p.Val365Asp
ENST00000706955.1:c.*1129_*1130delinsAT	ENSP00000516675.1:n.*1129_*1130delinsAT
ENST00000686459.1:c.*680_*681delinsAT	ENSP00000508909.1:n.*680_*681delinsAT
ENST00000688158.1:c.*1205_*1206delinsAT	ENSP00000509254.1:n.*1205_*1206delinsAT
ENST00000688308.1:c.1094_1095delinsAT	ENSP00000508752.1:p.Val365Asp
ENST00000688922.1:c.1015_1016delinsAT
ENST00000693560.1:c.1613_1614delinsAT	ENSP00000509861.1:p.Val538Asp
ENST00000371953.8:c.1094_1095delinsAT MANE Select	ENSP00000361021.3:p.Val365Asp
ENST00000371953.7:c.1094_1095delinsAT	ENSP00000361021.3:p.Val365Asp
NM_000314.5:c.1094_1095delinsAT	NP_000305.3:p.Val365Asp
NM_000314.6:c.1094_1095delinsAT	NP_000305.3:p.Val365Asp
NM_001304717.2:c.1613_1614delinsAT	NP_001291646.2:p.Val538Asp
NM_001304718.1:c.503_504delinsAT	NP_001291647.1:p.Val168Asp
XM_006717926.2:c.1049_1050delinsAT	XP_006717989.1:p.Val350Asp
XM_011539982.1:c.998_999delinsAT	XP_011538284.1:p.Val333Asp
XR_945791.1:n.1664_1665delinsAT
NM_000314.7:c.1094_1095delinsAT	NP_000305.3:p.Val365Asp
NM_001304717.5:c.1613_1614delinsAT	NP_001291646.4:p.Val538Asp
NM_001304718.2:c.503_504delinsAT	NP_001291647.1:p.Val168Asp
NM_000314.8:c.1094_1095delinsAT MANE Select	NP_000305.3:p.Val365Asp