Canonical Allele Identifier: CA377487299

Gene: PTEN

Linked Data

• ClinVar Variation Id: 651164
• ClinVar RCV Id: RCV000806464
• dbSNP Id: rs1589669344
• MyVariant Identifiers: chr10:g.89725141A>G (hg19) ; chr10:g.87965384A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965384A>G , CM000672.2:g.87965384A>G	GRCh38
NC_000010.10:g.89725141A>G , CM000672.1:g.89725141A>G	GRCh37
NC_000010.9:g.89715121A>G	NCBI36
NG_007466.2:g.106946A>G , LRG_311:g.106946A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1217A>G	ENSP00000514759.2:p.Asp406Gly
ENST00000710265.1:c.*153A>G	ENSP00000518161.1:n.*153A>G
ENST00000688158.2:n.1859A>G
ENST00000688922.2:c.*954A>G	ENSP00000508742.2:n.*954A>G
ENST00000700021.1:c.1079A>G	ENSP00000514757.1:p.Asp360Gly
ENST00000700022.1:c.*463A>G	ENSP00000514758.1:n.*463A>G
ENST00000700023.1:n.2282A>G
ENST00000700024.1:n.2516A>G
ENST00000706954.1:c.1124A>G	ENSP00000516674.1:p.Asp375Gly
ENST00000706955.1:c.*1159A>G	ENSP00000516675.1:n.*1159A>G
ENST00000686459.1:c.*710A>G	ENSP00000508909.1:n.*710A>G
ENST00000688158.1:c.*1235A>G	ENSP00000509254.1:n.*1235A>G
ENST00000688308.1:c.1124A>G	ENSP00000508752.1:p.Asp375Gly
ENST00000688922.1:c.1045A>G
ENST00000693560.1:c.1643A>G	ENSP00000509861.1:p.Asp548Gly
ENST00000371953.8:c.1124A>G MANE Select	ENSP00000361021.3:p.Asp375Gly
ENST00000371953.7:c.1124A>G	ENSP00000361021.3:p.Asp375Gly
NM_000314.5:c.1124A>G	NP_000305.3:p.Asp375Gly
NM_000314.6:c.1124A>G	NP_000305.3:p.Asp375Gly
NM_001304717.2:c.1643A>G	NP_001291646.2:p.Asp548Gly
NM_001304718.1:c.533A>G	NP_001291647.1:p.Asp178Gly
XM_006717926.2:c.1079A>G	XP_006717989.1:p.Asp360Gly
XM_011539982.1:c.1028A>G	XP_011538284.1:p.Asp343Gly
XR_945791.1:n.1694A>G
NM_000314.7:c.1124A>G	NP_000305.3:p.Asp375Gly
NM_001304717.5:c.1643A>G	NP_001291646.4:p.Asp548Gly
NM_001304718.2:c.533A>G	NP_001291647.1:p.Asp178Gly
NM_000314.8:c.1124A>G MANE Select	NP_000305.3:p.Asp375Gly