Canonical Allele Identifier: CA891841594

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965353_87965354delinsAC , CM000672.2:g.87965353_87965354delinsAC	GRCh38
NC_000010.10:g.89725110_89725111delinsAC , CM000672.1:g.89725110_89725111delinsAC	GRCh37
NC_000010.9:g.89715090_89715091delinsAC	NCBI36
NG_007466.2:g.106915_106916delinsAC , LRG_311:g.106915_106916delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1186_1187delinsAC	ENSP00000514759.2:p.Val396Thr
ENST00000710265.1:c.*122_*123delinsAC	ENSP00000518161.1:n.*122_*123delinsAC
ENST00000688158.2:n.1828_1829delinsAC
ENST00000688922.2:c.*923_*924delinsAC	ENSP00000508742.2:n.*923_*924delinsAC
ENST00000700021.1:c.1048_1049delinsAC	ENSP00000514757.1:p.Val350Thr
ENST00000700022.1:c.*432_*433delinsAC	ENSP00000514758.1:n.*432_*433delinsAC
ENST00000700023.1:n.2251_2252delinsAC
ENST00000700024.1:n.2485_2486delinsAC
ENST00000706954.1:c.1093_1094delinsAC	ENSP00000516674.1:p.Val365Thr
ENST00000706955.1:c.*1128_*1129delinsAC	ENSP00000516675.1:n.*1128_*1129delinsAC
ENST00000686459.1:c.*679_*680delinsAC	ENSP00000508909.1:n.*679_*680delinsAC
ENST00000688158.1:c.*1204_*1205delinsAC	ENSP00000509254.1:n.*1204_*1205delinsAC
ENST00000688308.1:c.1093_1094delinsAC	ENSP00000508752.1:p.Val365Thr
ENST00000688922.1:c.1014_1015delinsAC
ENST00000693560.1:c.1612_1613delinsAC	ENSP00000509861.1:p.Val538Thr
ENST00000371953.8:c.1093_1094delinsAC MANE Select	ENSP00000361021.3:p.Val365Thr
ENST00000371953.7:c.1093_1094delinsAC	ENSP00000361021.3:p.Val365Thr
NM_000314.5:c.1093_1094delinsAC	NP_000305.3:p.Val365Thr
NM_000314.6:c.1093_1094delinsAC	NP_000305.3:p.Val365Thr
NM_001304717.2:c.1612_1613delinsAC	NP_001291646.2:p.Val538Thr
NM_001304718.1:c.502_503delinsAC	NP_001291647.1:p.Val168Thr
XM_006717926.2:c.1048_1049delinsAC	XP_006717989.1:p.Val350Thr
XM_011539982.1:c.997_998delinsAC	XP_011538284.1:p.Val333Thr
XR_945791.1:n.1663_1664delinsAC
NM_000314.7:c.1093_1094delinsAC	NP_000305.3:p.Val365Thr
NM_001304717.5:c.1612_1613delinsAC	NP_001291646.4:p.Val538Thr
NM_001304718.2:c.502_503delinsAC	NP_001291647.1:p.Val168Thr
NM_000314.8:c.1093_1094delinsAC MANE Select	NP_000305.3:p.Val365Thr