Canonical Allele Identifier: CA891838108

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965437_87965438delinsTC , CM000672.2:g.87965437_87965438delinsTC	GRCh38
NC_000010.10:g.89725194_89725195delinsTC , CM000672.1:g.89725194_89725195delinsTC	GRCh37
NC_000010.9:g.89715174_89715175delinsTC	NCBI36
NG_007466.2:g.106999_107000delinsTC , LRG_311:g.106999_107000delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1270_1271delinsTC	ENSP00000514759.2:p.Asp424Ser
ENST00000710265.1:c.*206_*207delinsTC	ENSP00000518161.1:n.*206_*207delinsTC
ENST00000688158.2:n.1912_1913delinsTC
ENST00000688922.2:c.*1007_*1008delinsTC	ENSP00000508742.2:n.*1007_*1008delinsTC
ENST00000700021.1:c.1132_1133delinsTC	ENSP00000514757.1:p.Asp378Ser
ENST00000700022.1:c.*516_*517delinsTC	ENSP00000514758.1:n.*516_*517delinsTC
ENST00000700023.1:n.2335_2336delinsTC
ENST00000700024.1:n.2569_2570delinsTC
ENST00000706954.1:c.1177_1178delinsTC	ENSP00000516674.1:p.Asp393Ser
ENST00000706955.1:c.*1212_*1213delinsTC	ENSP00000516675.1:n.*1212_*1213delinsTC
ENST00000686459.1:c.*763_*764delinsTC	ENSP00000508909.1:n.*763_*764delinsTC
ENST00000688158.1:c.*1288_*1289delinsTC	ENSP00000509254.1:n.*1288_*1289delinsTC
ENST00000688308.1:c.1177_1178delinsTC	ENSP00000508752.1:p.Asp393Ser
ENST00000688922.1:c.1098_1099delinsTC
ENST00000693560.1:c.1696_1697delinsTC	ENSP00000509861.1:p.Asp566Ser
ENST00000371953.8:c.1177_1178delinsTC MANE Select	ENSP00000361021.3:p.Asp393Ser
ENST00000371953.7:c.1177_1178delinsTC	ENSP00000361021.3:p.Asp393Ser
NM_000314.5:c.1177_1178delinsTC	NP_000305.3:p.Asp393Ser
NM_000314.6:c.1177_1178delinsTC	NP_000305.3:p.Asp393Ser
NM_001304717.2:c.1696_1697delinsTC	NP_001291646.2:p.Asp566Ser
NM_001304718.1:c.586_587delinsTC	NP_001291647.1:p.Asp196Ser
XM_006717926.2:c.1132_1133delinsTC	XP_006717989.1:p.Asp378Ser
XM_011539982.1:c.1081_1082delinsTC	XP_011538284.1:p.Asp361Ser
XR_945791.1:n.1747_1748delinsTC
NM_000314.7:c.1177_1178delinsTC	NP_000305.3:p.Asp393Ser
NM_001304717.5:c.1696_1697delinsTC	NP_001291646.4:p.Asp566Ser
NM_001304718.2:c.586_587delinsTC	NP_001291647.1:p.Asp196Ser
NM_000314.8:c.1177_1178delinsTC MANE Select	NP_000305.3:p.Asp393Ser