Canonical Allele Identifier: CA470671157

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725112A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965355A>T , CM000672.2:g.87965355A>T	GRCh38
NC_000010.10:g.89725112A>T , CM000672.1:g.89725112A>T	GRCh37
NC_000010.9:g.89715092A>T	NCBI36
NG_007466.2:g.106917A>T , LRG_311:g.106917A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1188A>T	ENSP00000514759.2:p.Val396=
ENST00000710265.1:c.*124A>T	ENSP00000518161.1:n.*124A>T
ENST00000688158.2:n.1830A>T
ENST00000688922.2:c.*925A>T	ENSP00000508742.2:n.*925A>T
ENST00000700021.1:c.1050A>T	ENSP00000514757.1:p.Val350=
ENST00000700022.1:c.*434A>T	ENSP00000514758.1:n.*434A>T
ENST00000700023.1:n.2253A>T
ENST00000700024.1:n.2487A>T
ENST00000706954.1:c.1095A>T	ENSP00000516674.1:p.Val365=
ENST00000706955.1:c.*1130A>T	ENSP00000516675.1:n.*1130A>T
ENST00000686459.1:c.*681A>T	ENSP00000508909.1:n.*681A>T
ENST00000688158.1:c.*1206A>T	ENSP00000509254.1:n.*1206A>T
ENST00000688308.1:c.1095A>T	ENSP00000508752.1:p.Val365=
ENST00000688922.1:c.1016A>T
ENST00000693560.1:c.1614A>T	ENSP00000509861.1:p.Val538=
ENST00000371953.8:c.1095A>T MANE Select	ENSP00000361021.3:p.Val365=
ENST00000371953.7:c.1095A>T	ENSP00000361021.3:p.Val365=
NM_000314.5:c.1095A>T	NP_000305.3:p.Val365=
NM_000314.6:c.1095A>T	NP_000305.3:p.Val365=
NM_001304717.2:c.1614A>T	NP_001291646.2:p.Val538=
NM_001304718.1:c.504A>T	NP_001291647.1:p.Val168=
XM_006717926.2:c.1050A>T	XP_006717989.1:p.Val350=
XM_011539982.1:c.999A>T	XP_011538284.1:p.Val333=
XR_945791.1:n.1665A>T
NM_000314.7:c.1095A>T	NP_000305.3:p.Val365=
NM_001304717.5:c.1614A>T	NP_001291646.4:p.Val538=
NM_001304718.2:c.504A>T	NP_001291647.1:p.Val168=
NM_000314.8:c.1095A>T MANE Select	NP_000305.3:p.Val365=