Canonical Allele Identifier: CA891837385

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965344_87965346delinsGGT , CM000672.2:g.87965344_87965346delinsGGT	GRCh38
NC_000010.10:g.89725101_89725103delinsGGT , CM000672.1:g.89725101_89725103delinsGGT	GRCh37
NC_000010.9:g.89715081_89715083delinsGGT	NCBI36
NG_007466.2:g.106906_106908delinsGGT , LRG_311:g.106906_106908delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1177_1179delinsGGT	ENSP00000514759.2:p.Ser393Gly
ENST00000710265.1:c.*113_*115delinsGGT	ENSP00000518161.1:n.*113_*115delinsGGT
ENST00000688158.2:n.1819_1821delinsGGT
ENST00000688922.2:c.*914_*916delinsGGT	ENSP00000508742.2:n.*914_*916delinsGGT
ENST00000700021.1:c.1039_1041delinsGGT	ENSP00000514757.1:p.Ser347Gly
ENST00000700022.1:c.*423_*425delinsGGT	ENSP00000514758.1:n.*423_*425delinsGGT
ENST00000700023.1:n.2242_2244delinsGGT
ENST00000700024.1:n.2476_2478delinsGGT
ENST00000706954.1:c.1084_1086delinsGGT	ENSP00000516674.1:p.Ser362Gly
ENST00000706955.1:c.*1119_*1121delinsGGT	ENSP00000516675.1:n.*1119_*1121delinsGGT
ENST00000686459.1:c.*670_*672delinsGGT	ENSP00000508909.1:n.*670_*672delinsGGT
ENST00000688158.1:c.*1195_*1197delinsGGT	ENSP00000509254.1:n.*1195_*1197delinsGGT
ENST00000688308.1:c.1084_1086delinsGGT	ENSP00000508752.1:p.Ser362Gly
ENST00000688922.1:c.1005_1007delinsGGT
ENST00000693560.1:c.1603_1605delinsGGT	ENSP00000509861.1:p.Ser535Gly
ENST00000371953.8:c.1084_1086delinsGGT MANE Select	ENSP00000361021.3:p.Ser362Gly
ENST00000371953.7:c.1084_1086delinsGGT	ENSP00000361021.3:p.Ser362Gly
NM_000314.5:c.1084_1086delinsGGT	NP_000305.3:p.Ser362Gly
NM_000314.6:c.1084_1086delinsGGT	NP_000305.3:p.Ser362Gly
NM_001304717.2:c.1603_1605delinsGGT	NP_001291646.2:p.Ser535Gly
NM_001304718.1:c.493_495delinsGGT	NP_001291647.1:p.Ser165Gly
XM_006717926.2:c.1039_1041delinsGGT	XP_006717989.1:p.Ser347Gly
XM_011539982.1:c.988_990delinsGGT	XP_011538284.1:p.Ser330Gly
XR_945791.1:n.1654_1656delinsGGT
NM_000314.7:c.1084_1086delinsGGT	NP_000305.3:p.Ser362Gly
NM_001304717.5:c.1603_1605delinsGGT	NP_001291646.4:p.Ser535Gly
NM_001304718.2:c.493_495delinsGGT	NP_001291647.1:p.Ser165Gly
NM_000314.8:c.1084_1086delinsGGT MANE Select	NP_000305.3:p.Ser362Gly