Canonical Allele Identifier: CA891841673

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965437_87965438delinsAC , CM000672.2:g.87965437_87965438delinsAC	GRCh38
NC_000010.10:g.89725194_89725195delinsAC , CM000672.1:g.89725194_89725195delinsAC	GRCh37
NC_000010.9:g.89715174_89715175delinsAC	NCBI36
NG_007466.2:g.106999_107000delinsAC , LRG_311:g.106999_107000delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1270_1271delinsAC	ENSP00000514759.2:p.Asp424Thr
ENST00000710265.1:c.*206_*207delinsAC	ENSP00000518161.1:n.*206_*207delinsAC
ENST00000688158.2:n.1912_1913delinsAC
ENST00000688922.2:c.*1007_*1008delinsAC	ENSP00000508742.2:n.*1007_*1008delinsAC
ENST00000700021.1:c.1132_1133delinsAC	ENSP00000514757.1:p.Asp378Thr
ENST00000700022.1:c.*516_*517delinsAC	ENSP00000514758.1:n.*516_*517delinsAC
ENST00000700023.1:n.2335_2336delinsAC
ENST00000700024.1:n.2569_2570delinsAC
ENST00000706954.1:c.1177_1178delinsAC	ENSP00000516674.1:p.Asp393Thr
ENST00000706955.1:c.*1212_*1213delinsAC	ENSP00000516675.1:n.*1212_*1213delinsAC
ENST00000686459.1:c.*763_*764delinsAC	ENSP00000508909.1:n.*763_*764delinsAC
ENST00000688158.1:c.*1288_*1289delinsAC	ENSP00000509254.1:n.*1288_*1289delinsAC
ENST00000688308.1:c.1177_1178delinsAC	ENSP00000508752.1:p.Asp393Thr
ENST00000688922.1:c.1098_1099delinsAC
ENST00000693560.1:c.1696_1697delinsAC	ENSP00000509861.1:p.Asp566Thr
ENST00000371953.8:c.1177_1178delinsAC MANE Select	ENSP00000361021.3:p.Asp393Thr
ENST00000371953.7:c.1177_1178delinsAC	ENSP00000361021.3:p.Asp393Thr
NM_000314.5:c.1177_1178delinsAC	NP_000305.3:p.Asp393Thr
NM_000314.6:c.1177_1178delinsAC	NP_000305.3:p.Asp393Thr
NM_001304717.2:c.1696_1697delinsAC	NP_001291646.2:p.Asp566Thr
NM_001304718.1:c.586_587delinsAC	NP_001291647.1:p.Asp196Thr
XM_006717926.2:c.1132_1133delinsAC	XP_006717989.1:p.Asp378Thr
XM_011539982.1:c.1081_1082delinsAC	XP_011538284.1:p.Asp361Thr
XR_945791.1:n.1747_1748delinsAC
NM_000314.7:c.1177_1178delinsAC	NP_000305.3:p.Asp393Thr
NM_001304717.5:c.1696_1697delinsAC	NP_001291646.4:p.Asp566Thr
NM_001304718.2:c.586_587delinsAC	NP_001291647.1:p.Asp196Thr
NM_000314.8:c.1177_1178delinsAC MANE Select	NP_000305.3:p.Asp393Thr