Canonical Allele Identifier: CA470671203

Gene: PTEN

Linked Data

• dbSNP Id: rs2132289693
• MyVariant Identifiers: chr10:g.89725118A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965361A>T , CM000672.2:g.87965361A>T	GRCh38
NC_000010.10:g.89725118A>T , CM000672.1:g.89725118A>T	GRCh37
NC_000010.9:g.89715098A>T	NCBI36
NG_007466.2:g.106923A>T , LRG_311:g.106923A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1194A>T	ENSP00000514759.2:p.Pro398=
ENST00000710265.1:c.*130A>T	ENSP00000518161.1:n.*130A>T
ENST00000688158.2:n.1836A>T
ENST00000688922.2:c.*931A>T	ENSP00000508742.2:n.*931A>T
ENST00000700021.1:c.1056A>T	ENSP00000514757.1:p.Pro352=
ENST00000700022.1:c.*440A>T	ENSP00000514758.1:n.*440A>T
ENST00000700023.1:n.2259A>T
ENST00000700024.1:n.2493A>T
ENST00000706954.1:c.1101A>T	ENSP00000516674.1:p.Pro367=
ENST00000706955.1:c.*1136A>T	ENSP00000516675.1:n.*1136A>T
ENST00000686459.1:c.*687A>T	ENSP00000508909.1:n.*687A>T
ENST00000688158.1:c.*1212A>T	ENSP00000509254.1:n.*1212A>T
ENST00000688308.1:c.1101A>T	ENSP00000508752.1:p.Pro367=
ENST00000688922.1:c.1022A>T
ENST00000693560.1:c.1620A>T	ENSP00000509861.1:p.Pro540=
ENST00000371953.8:c.1101A>T MANE Select	ENSP00000361021.3:p.Pro367=
ENST00000371953.7:c.1101A>T	ENSP00000361021.3:p.Pro367=
NM_000314.5:c.1101A>T	NP_000305.3:p.Pro367=
NM_000314.6:c.1101A>T	NP_000305.3:p.Pro367=
NM_001304717.2:c.1620A>T	NP_001291646.2:p.Pro540=
NM_001304718.1:c.510A>T	NP_001291647.1:p.Pro170=
XM_006717926.2:c.1056A>T	XP_006717989.1:p.Pro352=
XM_011539982.1:c.1005A>T	XP_011538284.1:p.Pro335=
XR_945791.1:n.1671A>T
NM_000314.7:c.1101A>T	NP_000305.3:p.Pro367=
NM_001304717.5:c.1620A>T	NP_001291646.4:p.Pro540=
NM_001304718.2:c.510A>T	NP_001291647.1:p.Pro170=
NM_000314.8:c.1101A>T MANE Select	NP_000305.3:p.Pro367=