Canonical Allele Identifier: CA2579926447

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965344_87965346del , CM000672.2:g.87965344_87965346del	GRCh38
NC_000010.10:g.89725101_89725103del , CM000672.1:g.89725101_89725103del	GRCh37
NC_000010.9:g.89715081_89715083del	NCBI36
NG_007466.2:g.106906_106908del , LRG_311:g.106906_106908del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1177_1179del	ENSP00000514759.2:p.Ser393del
ENST00000710265.1:c.*113_*115del	ENSP00000518161.1:n.*113_*115del
ENST00000688158.2:n.1819_1821del
ENST00000688922.2:c.*914_*916del	ENSP00000508742.2:n.*914_*916del
ENST00000700021.1:c.1039_1041del	ENSP00000514757.1:p.Ser347del
ENST00000700022.1:c.*423_*425del	ENSP00000514758.1:n.*423_*425del
ENST00000700023.1:n.2242_2244del
ENST00000700024.1:n.2476_2478del
ENST00000706954.1:c.1084_1086del	ENSP00000516674.1:p.Ser362del
ENST00000706955.1:c.*1119_*1121del	ENSP00000516675.1:n.*1119_*1121del
ENST00000686459.1:c.*670_*672del	ENSP00000508909.1:n.*670_*672del
ENST00000688158.1:c.*1195_*1197del	ENSP00000509254.1:n.*1195_*1197del
ENST00000688308.1:c.1084_1086del	ENSP00000508752.1:p.Ser362del
ENST00000688922.1:c.1005_1007del
ENST00000693560.1:c.1603_1605del	ENSP00000509861.1:p.Ser535del
ENST00000371953.8:c.1084_1086del MANE Select	ENSP00000361021.3:p.Ser362del
ENST00000371953.7:c.1084_1086del	ENSP00000361021.3:p.Ser362del
NM_000314.5:c.1084_1086del	NP_000305.3:p.Ser362del
NM_000314.6:c.1084_1086del	NP_000305.3:p.Ser362del
NM_001304717.2:c.1603_1605del	NP_001291646.2:p.Ser535del
NM_001304718.1:c.493_495del	NP_001291647.1:p.Ser165del
XM_006717926.2:c.1039_1041del	XP_006717989.1:p.Ser347del
XM_011539982.1:c.988_990del	XP_011538284.1:p.Ser330del
XR_945791.1:n.1654_1656del
NM_000314.7:c.1084_1086del	NP_000305.3:p.Ser362del
NM_001304717.5:c.1603_1605del	NP_001291646.4:p.Ser535del
NM_001304718.2:c.493_495del	NP_001291647.1:p.Ser165del
NM_000314.8:c.1084_1086del MANE Select	NP_000305.3:p.Ser362del