Canonical Allele Identifier: CA470671101

Gene: PTEN

Linked Data

• dbSNP Id: rs761948873
• MyVariant Identifiers: chr10:g.89725103A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965346A>T , CM000672.2:g.87965346A>T	GRCh38
NC_000010.10:g.89725103A>T , CM000672.1:g.89725103A>T	GRCh37
NC_000010.9:g.89715083A>T	NCBI36
NG_007466.2:g.106908A>T , LRG_311:g.106908A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1179A>T	ENSP00000514759.2:p.Ser393=
ENST00000710265.1:c.*115A>T	ENSP00000518161.1:n.*115A>T
ENST00000688158.2:n.1821A>T
ENST00000688922.2:c.*916A>T	ENSP00000508742.2:n.*916A>T
ENST00000700021.1:c.1041A>T	ENSP00000514757.1:p.Ser347=
ENST00000700022.1:c.*425A>T	ENSP00000514758.1:n.*425A>T
ENST00000700023.1:n.2244A>T
ENST00000700024.1:n.2478A>T
ENST00000706954.1:c.1086A>T	ENSP00000516674.1:p.Ser362=
ENST00000706955.1:c.*1121A>T	ENSP00000516675.1:n.*1121A>T
ENST00000686459.1:c.*672A>T	ENSP00000508909.1:n.*672A>T
ENST00000688158.1:c.*1197A>T	ENSP00000509254.1:n.*1197A>T
ENST00000688308.1:c.1086A>T	ENSP00000508752.1:p.Ser362=
ENST00000688922.1:c.1007A>T
ENST00000693560.1:c.1605A>T	ENSP00000509861.1:p.Ser535=
ENST00000371953.8:c.1086A>T MANE Select	ENSP00000361021.3:p.Ser362=
ENST00000371953.7:c.1086A>T	ENSP00000361021.3:p.Ser362=
NM_000314.5:c.1086A>T	NP_000305.3:p.Ser362=
NM_000314.6:c.1086A>T	NP_000305.3:p.Ser362=
NM_001304717.2:c.1605A>T	NP_001291646.2:p.Ser535=
NM_001304718.1:c.495A>T	NP_001291647.1:p.Ser165=
XM_006717926.2:c.1041A>T	XP_006717989.1:p.Ser347=
XM_011539982.1:c.990A>T	XP_011538284.1:p.Ser330=
XR_945791.1:n.1656A>T
NM_000314.7:c.1086A>T	NP_000305.3:p.Ser362=
NM_001304717.5:c.1605A>T	NP_001291646.4:p.Ser535=
NM_001304718.2:c.495A>T	NP_001291647.1:p.Ser165=
NM_000314.8:c.1086A>T MANE Select	NP_000305.3:p.Ser362=