Canonical Allele Identifier: CA891834780
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960933_87960934delinsTA , CM000672.2:g.87960933_87960934delinsTA GRCh38
NC_000010.10:g.89720690_89720691delinsTA , CM000672.1:g.89720690_89720691delinsTA GRCh37
NC_000010.9:g.89710670_89710671delinsTA NCBI36
NG_007466.2:g.102495_102496delinsTA , LRG_311:g.102495_102496delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.934_935delinsTA ENSP00000514759.2:p.Pro312Ter
ENST00000710265.1:c.841_842delinsTA ENSP00000518161.1:p.Pro281Ter
ENST00000472832.3:c.841_842delinsTA ENSP00000483066.2:p.Pro281Ter
ENST00000688158.2:n.1576_1577delinsTA
ENST00000688922.2:c.*671_*672delinsTA ENSP00000508742.2:n.*671_*672delinsTA
ENST00000700021.1:c.796_797delinsTA ENSP00000514757.1:p.Pro266Ter
ENST00000700022.1:c.*180_*181delinsTA ENSP00000514758.1:n.*180_*181delinsTA
ENST00000700023.1:n.1999_2000delinsTA
ENST00000700024.1:n.2233_2234delinsTA
ENST00000700025.1:n.1610_1611delinsTA
ENST00000700026.1:n.478_479delinsTA
ENST00000700029.1:c.768_769delinsTA
ENST00000706954.1:c.841_842delinsTA ENSP00000516674.1:p.Pro281Ter
ENST00000706955.1:c.*876_*877delinsTA ENSP00000516675.1:n.*876_*877delinsTA
ENST00000686459.1:c.*427_*428delinsTA ENSP00000508909.1:n.*427_*428delinsTA
ENST00000688158.1:c.*952_*953delinsTA ENSP00000509254.1:n.*952_*953delinsTA
ENST00000688308.1:c.841_842delinsTA ENSP00000508752.1:p.Pro281Ter
ENST00000688922.1:c.762_763delinsTA
ENST00000693560.1:c.1360_1361delinsTA ENSP00000509861.1:p.Pro454Ter
ENST00000371953.8:c.841_842delinsTA MANE Select ENSP00000361021.3:p.Pro281Ter
ENST00000371953.7:c.841_842delinsTA ENSP00000361021.3:p.Pro281Ter
ENST00000472832.2:c.268_269delinsTA ENSP00000483066.1:p.Pro90Ter
NM_000314.5:c.841_842delinsTA NP_000305.3:p.Pro281Ter
NM_000314.6:c.841_842delinsTA NP_000305.3:p.Pro281Ter
NM_001304717.2:c.1360_1361delinsTA NP_001291646.2:p.Pro454Ter
NM_001304718.1:c.250_251delinsTA NP_001291647.1:p.Pro84Ter
XM_006717926.2:c.796_797delinsTA XP_006717989.1:p.Pro266Ter
XM_011539981.1:c.841_842delinsTA XP_011538283.1:p.Pro281Ter
XM_011539982.1:c.745_746delinsTA XP_011538284.1:p.Pro249Ter
XR_945791.1:n.1411_1412delinsTA
NM_000314.7:c.841_842delinsTA NP_000305.3:p.Pro281Ter
NM_001304717.5:c.1360_1361delinsTA NP_001291646.4:p.Pro454Ter
NM_001304718.2:c.250_251delinsTA NP_001291647.1:p.Pro84Ter
NM_000314.8:c.841_842delinsTA MANE Select NP_000305.3:p.Pro281Ter