Canonical Allele Identifier: CA891838145

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965443_87965444delinsAC , CM000672.2:g.87965443_87965444delinsAC	GRCh38
NC_000010.10:g.89725200_89725201delinsAC , CM000672.1:g.89725200_89725201delinsAC	GRCh37
NC_000010.9:g.89715180_89715181delinsAC	NCBI36
NG_007466.2:g.107005_107006delinsAC , LRG_311:g.107005_107006delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1276_1277delinsAC	ENSP00000514759.2:p.Asp426Thr
ENST00000710265.1:c.*212_*213delinsAC	ENSP00000518161.1:n.*212_*213delinsAC
ENST00000688158.2:n.1918_1919delinsAC
ENST00000688922.2:c.*1013_*1014delinsAC	ENSP00000508742.2:n.*1013_*1014delinsAC
ENST00000700021.1:c.1138_1139delinsAC	ENSP00000514757.1:p.Asp380Thr
ENST00000700022.1:c.*522_*523delinsAC	ENSP00000514758.1:n.*522_*523delinsAC
ENST00000700023.1:n.2341_2342delinsAC
ENST00000700024.1:n.2575_2576delinsAC
ENST00000706954.1:c.1183_1184delinsAC	ENSP00000516674.1:p.Asp395Thr
ENST00000706955.1:c.*1218_*1219delinsAC	ENSP00000516675.1:n.*1218_*1219delinsAC
ENST00000686459.1:c.*769_*770delinsAC	ENSP00000508909.1:n.*769_*770delinsAC
ENST00000688158.1:c.*1294_*1295delinsAC	ENSP00000509254.1:n.*1294_*1295delinsAC
ENST00000688308.1:c.1183_1184delinsAC	ENSP00000508752.1:p.Asp395Thr
ENST00000688922.1:c.1104_1105delinsAC
ENST00000693560.1:c.1702_1703delinsAC	ENSP00000509861.1:p.Asp568Thr
ENST00000371953.8:c.1183_1184delinsAC MANE Select	ENSP00000361021.3:p.Asp395Thr
ENST00000371953.7:c.1183_1184delinsAC	ENSP00000361021.3:p.Asp395Thr
NM_000314.5:c.1183_1184delinsAC	NP_000305.3:p.Asp395Thr
NM_000314.6:c.1183_1184delinsAC	NP_000305.3:p.Asp395Thr
NM_001304717.2:c.1702_1703delinsAC	NP_001291646.2:p.Asp568Thr
NM_001304718.1:c.592_593delinsAC	NP_001291647.1:p.Asp198Thr
XM_006717926.2:c.1138_1139delinsAC	XP_006717989.1:p.Asp380Thr
XM_011539982.1:c.1087_1088delinsAC	XP_011538284.1:p.Asp363Thr
XR_945791.1:n.1753_1754delinsAC
NM_000314.7:c.1183_1184delinsAC	NP_000305.3:p.Asp395Thr
NM_001304717.5:c.1702_1703delinsAC	NP_001291646.4:p.Asp568Thr
NM_001304718.2:c.592_593delinsAC	NP_001291647.1:p.Asp198Thr
NM_000314.8:c.1183_1184delinsAC MANE Select	NP_000305.3:p.Asp395Thr