Canonical Allele Identifier: CA377485078
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132277734

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958004C>G , CM000672.2:g.87958004C>G GRCh38
NC_000010.10:g.89717761C>G , CM000672.1:g.89717761C>G GRCh37
NC_000010.9:g.89707741C>G NCBI36
NG_007466.2:g.99566C>G , LRG_311:g.99566C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.786C>G ENSP00000514759.2:p.Asn262Lys
ENST00000710265.1:c.786C>G ENSP00000518161.1:p.Asn262Lys
ENST00000472832.3:c.786C>G ENSP00000483066.2:p.Asn262Lys
ENST00000688158.2:n.1521C>G
ENST00000688922.2:c.*616C>G ENSP00000508742.2:n.*616C>G
ENST00000700021.1:c.741C>G ENSP00000514757.1:p.Asn247Lys
ENST00000700022.1:c.*125C>G ENSP00000514758.1:n.*125C>G
ENST00000700023.1:n.1944C>G
ENST00000700024.1:n.2178C>G
ENST00000700025.1:n.1555C>G
ENST00000700026.1:n.423C>G
ENST00000700029.1:c.620C>G
ENST00000706954.1:c.786C>G ENSP00000516674.1:p.Asn262Lys
ENST00000706955.1:c.*821C>G ENSP00000516675.1:n.*821C>G
ENST00000686459.1:c.*372C>G ENSP00000508909.1:n.*372C>G
ENST00000688158.1:c.*897C>G ENSP00000509254.1:n.*897C>G
ENST00000688308.1:c.786C>G ENSP00000508752.1:p.Asn262Lys
ENST00000688922.1:c.707C>G
ENST00000693560.1:c.1305C>G ENSP00000509861.1:p.Asn435Lys
ENST00000371953.8:c.786C>G MANE Select ENSP00000361021.3:p.Asn262Lys
ENST00000371953.7:c.786C>G ENSP00000361021.3:p.Asn262Lys
ENST00000472832.2:c.213C>G ENSP00000483066.1:p.Asn71Lys
NM_000314.5:c.786C>G NP_000305.3:p.Asn262Lys
NM_000314.6:c.786C>G NP_000305.3:p.Asn262Lys
NM_001304717.2:c.1305C>G NP_001291646.2:p.Asn435Lys
NM_001304718.1:c.195C>G NP_001291647.1:p.Asn65Lys
XM_006717926.2:c.741C>G XP_006717989.1:p.Asn247Lys
XM_011539981.1:c.786C>G XP_011538283.1:p.Asn262Lys
XM_011539982.1:c.690C>G XP_011538284.1:p.Asn230Lys
XR_945791.1:n.1356C>G
NM_000314.7:c.786C>G NP_000305.3:p.Asn262Lys
NM_001304717.5:c.1305C>G NP_001291646.4:p.Asn435Lys
NM_001304718.2:c.195C>G NP_001291647.1:p.Asn65Lys
NM_000314.8:c.786C>G MANE Select NP_000305.3:p.Asn262Lys