Canonical Allele Identifier: CA891841735

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965467_87965468delinsAC , CM000672.2:g.87965467_87965468delinsAC	GRCh38
NC_000010.10:g.89725224_89725225delinsAC , CM000672.1:g.89725224_89725225delinsAC	GRCh37
NC_000010.9:g.89715204_89715205delinsAC	NCBI36
NG_007466.2:g.107029_107030delinsAC , LRG_311:g.107029_107030delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1300_1301delinsAC	ENSP00000514759.2:p.Val434Thr
ENST00000710265.1:c.*236_*237delinsAC	ENSP00000518161.1:n.*236_*237delinsAC
ENST00000688158.2:n.1942_1943delinsAC
ENST00000688922.2:c.*1037_*1038delinsAC	ENSP00000508742.2:n.*1037_*1038delinsAC
ENST00000700021.1:c.1162_1163delinsAC	ENSP00000514757.1:p.Val388Thr
ENST00000700022.1:c.*546_*547delinsAC	ENSP00000514758.1:n.*546_*547delinsAC
ENST00000700023.1:n.2365_2366delinsAC
ENST00000700024.1:n.2599_2600delinsAC
ENST00000706954.1:c.1207_1208delinsAC	ENSP00000516674.1:p.Val403Thr
ENST00000706955.1:c.*1242_*1243delinsAC	ENSP00000516675.1:n.*1242_*1243delinsAC
ENST00000686459.1:c.*793_*794delinsAC	ENSP00000508909.1:n.*793_*794delinsAC
ENST00000688158.1:c.*1318_*1319delinsAC	ENSP00000509254.1:n.*1318_*1319delinsAC
ENST00000688308.1:c.1207_1208delinsAC	ENSP00000508752.1:p.Val403Thr
ENST00000688922.1:c.1128_1129delinsAC
ENST00000693560.1:c.1726_1727delinsAC	ENSP00000509861.1:p.Val576Thr
ENST00000371953.8:c.1207_1208delinsAC MANE Select	ENSP00000361021.3:p.Val403Thr
ENST00000371953.7:c.1207_1208delinsAC	ENSP00000361021.3:p.Val403Thr
NM_000314.5:c.1207_1208delinsAC	NP_000305.3:p.Val403Thr
NM_000314.6:c.1207_1208delinsAC	NP_000305.3:p.Val403Thr
NM_001304717.2:c.1726_1727delinsAC	NP_001291646.2:p.Val576Thr
NM_001304718.1:c.616_617delinsAC	NP_001291647.1:p.Val206Thr
XM_006717926.2:c.1162_1163delinsAC	XP_006717989.1:p.Val388Thr
XM_011539982.1:c.1111_1112delinsAC	XP_011538284.1:p.Val371Thr
XR_945791.1:n.1777_1778delinsAC
NM_000314.7:c.1207_1208delinsAC	NP_000305.3:p.Val403Thr
NM_001304717.5:c.1726_1727delinsAC	NP_001291646.4:p.Val576Thr
NM_001304718.2:c.616_617delinsAC	NP_001291647.1:p.Val206Thr
NM_000314.8:c.1207_1208delinsAC MANE Select	NP_000305.3:p.Val403Thr