Canonical Allele Identifier: CA891837391

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965344_87965346delinsGCT , CM000672.2:g.87965344_87965346delinsGCT	GRCh38
NC_000010.10:g.89725101_89725103delinsGCT , CM000672.1:g.89725101_89725103delinsGCT	GRCh37
NC_000010.9:g.89715081_89715083delinsGCT	NCBI36
NG_007466.2:g.106906_106908delinsGCT , LRG_311:g.106906_106908delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1177_1179delinsGCT	ENSP00000514759.2:p.Ser393Ala
ENST00000710265.1:c.*113_*115delinsGCT	ENSP00000518161.1:n.*113_*115delinsGCT
ENST00000688158.2:n.1819_1821delinsGCT
ENST00000688922.2:c.*914_*916delinsGCT	ENSP00000508742.2:n.*914_*916delinsGCT
ENST00000700021.1:c.1039_1041delinsGCT	ENSP00000514757.1:p.Ser347Ala
ENST00000700022.1:c.*423_*425delinsGCT	ENSP00000514758.1:n.*423_*425delinsGCT
ENST00000700023.1:n.2242_2244delinsGCT
ENST00000700024.1:n.2476_2478delinsGCT
ENST00000706954.1:c.1084_1086delinsGCT	ENSP00000516674.1:p.Ser362Ala
ENST00000706955.1:c.*1119_*1121delinsGCT	ENSP00000516675.1:n.*1119_*1121delinsGCT
ENST00000686459.1:c.*670_*672delinsGCT	ENSP00000508909.1:n.*670_*672delinsGCT
ENST00000688158.1:c.*1195_*1197delinsGCT	ENSP00000509254.1:n.*1195_*1197delinsGCT
ENST00000688308.1:c.1084_1086delinsGCT	ENSP00000508752.1:p.Ser362Ala
ENST00000688922.1:c.1005_1007delinsGCT
ENST00000693560.1:c.1603_1605delinsGCT	ENSP00000509861.1:p.Ser535Ala
ENST00000371953.8:c.1084_1086delinsGCT MANE Select	ENSP00000361021.3:p.Ser362Ala
ENST00000371953.7:c.1084_1086delinsGCT	ENSP00000361021.3:p.Ser362Ala
NM_000314.5:c.1084_1086delinsGCT	NP_000305.3:p.Ser362Ala
NM_000314.6:c.1084_1086delinsGCT	NP_000305.3:p.Ser362Ala
NM_001304717.2:c.1603_1605delinsGCT	NP_001291646.2:p.Ser535Ala
NM_001304718.1:c.493_495delinsGCT	NP_001291647.1:p.Ser165Ala
XM_006717926.2:c.1039_1041delinsGCT	XP_006717989.1:p.Ser347Ala
XM_011539982.1:c.988_990delinsGCT	XP_011538284.1:p.Ser330Ala
XR_945791.1:n.1654_1656delinsGCT
NM_000314.7:c.1084_1086delinsGCT	NP_000305.3:p.Ser362Ala
NM_001304717.5:c.1603_1605delinsGCT	NP_001291646.4:p.Ser535Ala
NM_001304718.2:c.493_495delinsGCT	NP_001291647.1:p.Ser165Ala
NM_000314.8:c.1084_1086delinsGCT MANE Select	NP_000305.3:p.Ser362Ala