Canonical Allele Identifier: CA377485567
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132281980

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960934C>G , CM000672.2:g.87960934C>G GRCh38
NC_000010.10:g.89720691C>G , CM000672.1:g.89720691C>G GRCh37
NC_000010.9:g.89710671C>G NCBI36
NG_007466.2:g.102496C>G , LRG_311:g.102496C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.935C>G ENSP00000514759.2:p.Pro312Arg
ENST00000710265.1:c.842C>G ENSP00000518161.1:p.Pro281Arg
ENST00000472832.3:c.842C>G ENSP00000483066.2:p.Pro281Arg
ENST00000688158.2:n.1577C>G
ENST00000688922.2:c.*672C>G ENSP00000508742.2:n.*672C>G
ENST00000700021.1:c.797C>G ENSP00000514757.1:p.Pro266Arg
ENST00000700022.1:c.*181C>G ENSP00000514758.1:n.*181C>G
ENST00000700023.1:n.2000C>G
ENST00000700024.1:n.2234C>G
ENST00000700025.1:n.1611C>G
ENST00000700026.1:n.479C>G
ENST00000700029.1:c.769C>G
ENST00000706954.1:c.842C>G ENSP00000516674.1:p.Pro281Arg
ENST00000706955.1:c.*877C>G ENSP00000516675.1:n.*877C>G
ENST00000686459.1:c.*428C>G ENSP00000508909.1:n.*428C>G
ENST00000688158.1:c.*953C>G ENSP00000509254.1:n.*953C>G
ENST00000688308.1:c.842C>G ENSP00000508752.1:p.Pro281Arg
ENST00000688922.1:c.763C>G
ENST00000693560.1:c.1361C>G ENSP00000509861.1:p.Pro454Arg
ENST00000371953.8:c.842C>G MANE Select ENSP00000361021.3:p.Pro281Arg
ENST00000371953.7:c.842C>G ENSP00000361021.3:p.Pro281Arg
ENST00000472832.2:c.269C>G ENSP00000483066.1:p.Pro90Arg
NM_000314.5:c.842C>G NP_000305.3:p.Pro281Arg
NM_000314.6:c.842C>G NP_000305.3:p.Pro281Arg
NM_001304717.2:c.1361C>G NP_001291646.2:p.Pro454Arg
NM_001304718.1:c.251C>G NP_001291647.1:p.Pro84Arg
XM_006717926.2:c.797C>G XP_006717989.1:p.Pro266Arg
XM_011539981.1:c.842C>G XP_011538283.1:p.Pro281Arg
XM_011539982.1:c.746C>G XP_011538284.1:p.Pro249Arg
XR_945791.1:n.1412C>G
NM_000314.7:c.842C>G NP_000305.3:p.Pro281Arg
NM_001304717.5:c.1361C>G NP_001291646.4:p.Pro454Arg
NM_001304718.2:c.251C>G NP_001291647.1:p.Pro84Arg
NM_000314.8:c.842C>G MANE Select NP_000305.3:p.Pro281Arg