Canonical Allele Identifier: CA377484261

Gene: PTEN

Linked Data

• dbSNP Id: rs1564837747
• MyVariant Identifiers: chr10:g.89711887C>A (hg19) ; chr10:g.87952130C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952130C>A , CM000672.2:g.87952130C>A	GRCh38
NC_000010.10:g.89711887C>A , CM000672.1:g.89711887C>A	GRCh37
NC_000010.9:g.89701867C>A	NCBI36
NG_007466.2:g.93692C>A , LRG_311:g.93692C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.505C>A	ENSP00000514759.2:p.Pro169Thr
ENST00000710265.1:c.505C>A	ENSP00000518161.1:p.Pro169Thr
ENST00000472832.3:c.505C>A	ENSP00000483066.2:p.Pro169Thr
ENST00000688158.2:n.1240C>A
ENST00000688922.2:c.*335C>A	ENSP00000508742.2:n.*335C>A
ENST00000700021.1:c.460C>A	ENSP00000514757.1:p.Pro154Thr
ENST00000700022.1:c.493-5723C>A	ENSP00000514758.1:n.493-5723C>A
ENST00000700023.1:n.1663C>A
ENST00000700024.1:n.1897C>A
ENST00000700025.1:n.1274C>A
ENST00000700029.1:c.339C>A
ENST00000706954.1:c.505C>A	ENSP00000516674.1:p.Pro169Thr
ENST00000706955.1:c.*540C>A	ENSP00000516675.1:n.*540C>A
ENST00000686459.1:c.*91C>A	ENSP00000508909.1:n.*91C>A
ENST00000688158.1:c.*616C>A	ENSP00000509254.1:n.*616C>A
ENST00000688308.1:c.505C>A	ENSP00000508752.1:p.Pro169Thr
ENST00000688922.1:c.426C>A
ENST00000693560.1:c.1024C>A	ENSP00000509861.1:p.Pro342Thr
ENST00000371953.8:c.505C>A MANE Select	ENSP00000361021.3:p.Pro169Thr
ENST00000371953.7:c.505C>A	ENSP00000361021.3:p.Pro169Thr
NM_000314.5:c.505C>A	NP_000305.3:p.Pro169Thr
NM_000314.6:c.505C>A	NP_000305.3:p.Pro169Thr
NM_001304717.2:c.1024C>A	NP_001291646.2:p.Pro342Thr
NM_001304718.1:c.-87C>A	NP_001291647.1:n.-87C>A
XM_006717926.2:c.460C>A	XP_006717989.1:p.Pro154Thr
XM_011539981.1:c.505C>A	XP_011538283.1:p.Pro169Thr
XM_011539982.1:c.409C>A	XP_011538284.1:p.Pro137Thr
XR_945789.1:n.1376C>A
XR_945790.1:n.1493C>A
XR_945791.1:n.1205-5723C>A
NM_000314.7:c.505C>A	NP_000305.3:p.Pro169Thr
NM_001304717.5:c.1024C>A	NP_001291646.4:p.Pro342Thr
NM_001304718.2:c.-87C>A	NP_001291647.1:n.-87C>A
NM_000314.8:c.505C>A MANE Select	NP_000305.3:p.Pro169Thr