Canonical Allele Identifier: CA470661384

Gene: PTEN

Linked Data

• dbSNP Id: rs746661067
• MyVariant Identifiers: chr10:g.89692804A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933047A>T , CM000672.2:g.87933047A>T	GRCh38
NC_000010.10:g.89692804A>T , CM000672.1:g.89692804A>T	GRCh37
NC_000010.9:g.89682784A>T	NCBI36
NG_007466.2:g.74609A>T , LRG_311:g.74609A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.288A>T	ENSP00000514759.2:p.Pro96=
ENST00000710265.1:c.288A>T	ENSP00000518161.1:p.Pro96=
ENST00000472832.3:c.288A>T	ENSP00000483066.2:p.Pro96=
ENST00000688158.2:n.1023A>T
ENST00000688922.2:c.*118A>T	ENSP00000508742.2:n.*118A>T
ENST00000700021.1:c.243A>T	ENSP00000514757.1:p.Pro81=
ENST00000700022.1:c.288A>T	ENSP00000514758.1:p.Pro96=
ENST00000700029.1:c.122A>T
ENST00000706954.1:c.288A>T	ENSP00000516674.1:p.Pro96=
ENST00000706955.1:c.*323A>T	ENSP00000516675.1:n.*323A>T
ENST00000686459.1:c.288A>T	ENSP00000508909.1:p.Pro96=
ENST00000688158.1:c.*399A>T	ENSP00000509254.1:n.*399A>T
ENST00000688308.1:c.288A>T	ENSP00000508752.1:p.Pro96=
ENST00000688922.1:c.209A>T
ENST00000693560.1:c.807A>T	ENSP00000509861.1:p.Pro269=
ENST00000371953.8:c.288A>T MANE Select	ENSP00000361021.3:p.Pro96=
ENST00000371953.7:c.288A>T	ENSP00000361021.3:p.Pro96=
ENST00000498703.1:n.114A>T
ENST00000610634.1:c.186A>T	ENSP00000477517.1:p.Pro62=
NM_000314.5:c.288A>T	NP_000305.3:p.Pro96=
NM_000314.6:c.288A>T	NP_000305.3:p.Pro96=
NM_001304717.2:c.807A>T	NP_001291646.2:p.Pro269=
NM_001304718.1:c.-463A>T	NP_001291647.1:n.-463A>T
XM_006717926.2:c.243A>T	XP_006717989.1:p.Pro81=
XM_011539981.1:c.288A>T	XP_011538283.1:p.Pro96=
XM_011539982.1:c.192A>T	XP_011538284.1:p.Pro64=
XR_945789.1:n.1000A>T
XR_945790.1:n.1000A>T
XR_945791.1:n.1000A>T
NM_000314.7:c.288A>T	NP_000305.3:p.Pro96=
NM_001304717.5:c.807A>T	NP_001291646.4:p.Pro269=
NM_001304718.2:c.-463A>T	NP_001291647.1:n.-463A>T
NM_000314.8:c.288A>T MANE Select	NP_000305.3:p.Pro96=