Canonical Allele Identifier: CA891837396

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965345_87965346delinsAT , CM000672.2:g.87965345_87965346delinsAT	GRCh38
NC_000010.10:g.89725102_89725103delinsAT , CM000672.1:g.89725102_89725103delinsAT	GRCh37
NC_000010.9:g.89715082_89715083delinsAT	NCBI36
NG_007466.2:g.106907_106908delinsAT , LRG_311:g.106907_106908delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1178_1179delinsAT	ENSP00000514759.2:p.Ser393Tyr
ENST00000710265.1:c.*114_*115delinsAT	ENSP00000518161.1:n.*114_*115delinsAT
ENST00000688158.2:n.1820_1821delinsAT
ENST00000688922.2:c.*915_*916delinsAT	ENSP00000508742.2:n.*915_*916delinsAT
ENST00000700021.1:c.1040_1041delinsAT	ENSP00000514757.1:p.Ser347Tyr
ENST00000700022.1:c.*424_*425delinsAT	ENSP00000514758.1:n.*424_*425delinsAT
ENST00000700023.1:n.2243_2244delinsAT
ENST00000700024.1:n.2477_2478delinsAT
ENST00000706954.1:c.1085_1086delinsAT	ENSP00000516674.1:p.Ser362Tyr
ENST00000706955.1:c.*1120_*1121delinsAT	ENSP00000516675.1:n.*1120_*1121delinsAT
ENST00000686459.1:c.*671_*672delinsAT	ENSP00000508909.1:n.*671_*672delinsAT
ENST00000688158.1:c.*1196_*1197delinsAT	ENSP00000509254.1:n.*1196_*1197delinsAT
ENST00000688308.1:c.1085_1086delinsAT	ENSP00000508752.1:p.Ser362Tyr
ENST00000688922.1:c.1006_1007delinsAT
ENST00000693560.1:c.1604_1605delinsAT	ENSP00000509861.1:p.Ser535Tyr
ENST00000371953.8:c.1085_1086delinsAT MANE Select	ENSP00000361021.3:p.Ser362Tyr
ENST00000371953.7:c.1085_1086delinsAT	ENSP00000361021.3:p.Ser362Tyr
NM_000314.5:c.1085_1086delinsAT	NP_000305.3:p.Ser362Tyr
NM_000314.6:c.1085_1086delinsAT	NP_000305.3:p.Ser362Tyr
NM_001304717.2:c.1604_1605delinsAT	NP_001291646.2:p.Ser535Tyr
NM_001304718.1:c.494_495delinsAT	NP_001291647.1:p.Ser165Tyr
XM_006717926.2:c.1040_1041delinsAT	XP_006717989.1:p.Ser347Tyr
XM_011539982.1:c.989_990delinsAT	XP_011538284.1:p.Ser330Tyr
XR_945791.1:n.1655_1656delinsAT
NM_000314.7:c.1085_1086delinsAT	NP_000305.3:p.Ser362Tyr
NM_001304717.5:c.1604_1605delinsAT	NP_001291646.4:p.Ser535Tyr
NM_001304718.2:c.494_495delinsAT	NP_001291647.1:p.Ser165Tyr
NM_000314.8:c.1085_1086delinsAT MANE Select	NP_000305.3:p.Ser362Tyr