Canonical Allele Identifier: CA891838175
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965447_87965448delinsCA , CM000672.2:g.87965447_87965448delinsCA GRCh38
NC_000010.10:g.89725204_89725205delinsCA , CM000672.1:g.89725204_89725205delinsCA GRCh37
NC_000010.9:g.89715184_89715185delinsCA NCBI36
NG_007466.2:g.107009_107010delinsCA , LRG_311:g.107009_107010delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1280_1281delinsCA ENSP00000514759.2:p.Gln427Pro
ENST00000710265.1:c.*216_*217delinsCA ENSP00000518161.1:n.*216_*217delinsCA
ENST00000688158.2:n.1922_1923delinsCA
ENST00000688922.2:c.*1017_*1018delinsCA ENSP00000508742.2:n.*1017_*1018delinsCA
ENST00000700021.1:c.1142_1143delinsCA ENSP00000514757.1:p.Gln381Pro
ENST00000700022.1:c.*526_*527delinsCA ENSP00000514758.1:n.*526_*527delinsCA
ENST00000700023.1:n.2345_2346delinsCA
ENST00000700024.1:n.2579_2580delinsCA
ENST00000706954.1:c.1187_1188delinsCA ENSP00000516674.1:p.Gln396Pro
ENST00000706955.1:c.*1222_*1223delinsCA ENSP00000516675.1:n.*1222_*1223delinsCA
ENST00000686459.1:c.*773_*774delinsCA ENSP00000508909.1:n.*773_*774delinsCA
ENST00000688158.1:c.*1298_*1299delinsCA ENSP00000509254.1:n.*1298_*1299delinsCA
ENST00000688308.1:c.1187_1188delinsCA ENSP00000508752.1:p.Gln396Pro
ENST00000688922.1:c.1108_1109delinsCA
ENST00000693560.1:c.1706_1707delinsCA ENSP00000509861.1:p.Gln569Pro
ENST00000371953.8:c.1187_1188delinsCA MANE Select ENSP00000361021.3:p.Gln396Pro
ENST00000371953.7:c.1187_1188delinsCA ENSP00000361021.3:p.Gln396Pro
NM_000314.5:c.1187_1188delinsCA NP_000305.3:p.Gln396Pro
NM_000314.6:c.1187_1188delinsCA NP_000305.3:p.Gln396Pro
NM_001304717.2:c.1706_1707delinsCA NP_001291646.2:p.Gln569Pro
NM_001304718.1:c.596_597delinsCA NP_001291647.1:p.Gln199Pro
XM_006717926.2:c.1142_1143delinsCA XP_006717989.1:p.Gln381Pro
XM_011539982.1:c.1091_1092delinsCA XP_011538284.1:p.Gln364Pro
XR_945791.1:n.1757_1758delinsCA
NM_000314.7:c.1187_1188delinsCA NP_000305.3:p.Gln396Pro
NM_001304717.5:c.1706_1707delinsCA NP_001291646.4:p.Gln569Pro
NM_001304718.2:c.596_597delinsCA NP_001291647.1:p.Gln199Pro
NM_000314.8:c.1187_1188delinsCA MANE Select NP_000305.3:p.Gln396Pro