Canonical Allele Identifier: CA891841696
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965446_87965447delinsGC , CM000672.2:g.87965446_87965447delinsGC GRCh38
NC_000010.10:g.89725203_89725204delinsGC , CM000672.1:g.89725203_89725204delinsGC GRCh37
NC_000010.9:g.89715183_89715184delinsGC NCBI36
NG_007466.2:g.107008_107009delinsGC , LRG_311:g.107008_107009delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1279_1280delinsGC ENSP00000514759.2:p.Gln427Ala
ENST00000710265.1:c.*215_*216delinsGC ENSP00000518161.1:n.*215_*216delinsGC
ENST00000688158.2:n.1921_1922delinsGC
ENST00000688922.2:c.*1016_*1017delinsGC ENSP00000508742.2:n.*1016_*1017delinsGC
ENST00000700021.1:c.1141_1142delinsGC ENSP00000514757.1:p.Gln381Ala
ENST00000700022.1:c.*525_*526delinsGC ENSP00000514758.1:n.*525_*526delinsGC
ENST00000700023.1:n.2344_2345delinsGC
ENST00000700024.1:n.2578_2579delinsGC
ENST00000706954.1:c.1186_1187delinsGC ENSP00000516674.1:p.Gln396Ala
ENST00000706955.1:c.*1221_*1222delinsGC ENSP00000516675.1:n.*1221_*1222delinsGC
ENST00000686459.1:c.*772_*773delinsGC ENSP00000508909.1:n.*772_*773delinsGC
ENST00000688158.1:c.*1297_*1298delinsGC ENSP00000509254.1:n.*1297_*1298delinsGC
ENST00000688308.1:c.1186_1187delinsGC ENSP00000508752.1:p.Gln396Ala
ENST00000688922.1:c.1107_1108delinsGC
ENST00000693560.1:c.1705_1706delinsGC ENSP00000509861.1:p.Gln569Ala
ENST00000371953.8:c.1186_1187delinsGC MANE Select ENSP00000361021.3:p.Gln396Ala
ENST00000371953.7:c.1186_1187delinsGC ENSP00000361021.3:p.Gln396Ala
NM_000314.5:c.1186_1187delinsGC NP_000305.3:p.Gln396Ala
NM_000314.6:c.1186_1187delinsGC NP_000305.3:p.Gln396Ala
NM_001304717.2:c.1705_1706delinsGC NP_001291646.2:p.Gln569Ala
NM_001304718.1:c.595_596delinsGC NP_001291647.1:p.Gln199Ala
XM_006717926.2:c.1141_1142delinsGC XP_006717989.1:p.Gln381Ala
XM_011539982.1:c.1090_1091delinsGC XP_011538284.1:p.Gln364Ala
XR_945791.1:n.1756_1757delinsGC
NM_000314.7:c.1186_1187delinsGC NP_000305.3:p.Gln396Ala
NM_001304717.5:c.1705_1706delinsGC NP_001291646.4:p.Gln569Ala
NM_001304718.2:c.595_596delinsGC NP_001291647.1:p.Gln199Ala
NM_000314.8:c.1186_1187delinsGC MANE Select NP_000305.3:p.Gln396Ala