Canonical Allele Identifier: CA470667567

Gene: PTEN

Linked Data

• dbSNP Id: rs2132269001
• MyVariant Identifiers: chr10:g.89711889C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952132C>G , CM000672.2:g.87952132C>G	GRCh38
NC_000010.10:g.89711889C>G , CM000672.1:g.89711889C>G	GRCh37
NC_000010.9:g.89701869C>G	NCBI36
NG_007466.2:g.93694C>G , LRG_311:g.93694C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.507C>G	ENSP00000514759.2:p.Pro169=
ENST00000710265.1:c.507C>G	ENSP00000518161.1:p.Pro169=
ENST00000472832.3:c.507C>G	ENSP00000483066.2:p.Pro169=
ENST00000688158.2:n.1242C>G
ENST00000688922.2:c.*337C>G	ENSP00000508742.2:n.*337C>G
ENST00000700021.1:c.462C>G	ENSP00000514757.1:p.Pro154=
ENST00000700022.1:c.493-5721C>G	ENSP00000514758.1:n.493-5721C>G
ENST00000700023.1:n.1665C>G
ENST00000700024.1:n.1899C>G
ENST00000700025.1:n.1276C>G
ENST00000700029.1:c.341C>G
ENST00000706954.1:c.507C>G	ENSP00000516674.1:p.Pro169=
ENST00000706955.1:c.*542C>G	ENSP00000516675.1:n.*542C>G
ENST00000686459.1:c.*93C>G	ENSP00000508909.1:n.*93C>G
ENST00000688158.1:c.*618C>G	ENSP00000509254.1:n.*618C>G
ENST00000688308.1:c.507C>G	ENSP00000508752.1:p.Pro169=
ENST00000688922.1:c.428C>G
ENST00000693560.1:c.1026C>G	ENSP00000509861.1:p.Pro342=
ENST00000371953.8:c.507C>G MANE Select	ENSP00000361021.3:p.Pro169=
ENST00000371953.7:c.507C>G	ENSP00000361021.3:p.Pro169=
NM_000314.5:c.507C>G	NP_000305.3:p.Pro169=
NM_000314.6:c.507C>G	NP_000305.3:p.Pro169=
NM_001304717.2:c.1026C>G	NP_001291646.2:p.Pro342=
NM_001304718.1:c.-85C>G	NP_001291647.1:n.-85C>G
XM_006717926.2:c.462C>G	XP_006717989.1:p.Pro154=
XM_011539981.1:c.507C>G	XP_011538283.1:p.Pro169=
XM_011539982.1:c.411C>G	XP_011538284.1:p.Pro137=
XR_945789.1:n.1378C>G
XR_945790.1:n.1495C>G
XR_945791.1:n.1205-5721C>G
NM_000314.7:c.507C>G	NP_000305.3:p.Pro169=
NM_001304717.5:c.1026C>G	NP_001291646.4:p.Pro342=
NM_001304718.2:c.-85C>G	NP_001291647.1:n.-85C>G
NM_000314.8:c.507C>G MANE Select	NP_000305.3:p.Pro169=