Canonical Allele Identifier: CA891836242
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961023_87961025delinsCCA , CM000672.2:g.87961023_87961025delinsCCA GRCh38
NC_000010.10:g.89720780_89720782delinsCCA , CM000672.1:g.89720780_89720782delinsCCA GRCh37
NC_000010.9:g.89710760_89710762delinsCCA NCBI36
NG_007466.2:g.102585_102587delinsCCA , LRG_311:g.102585_102587delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1024_1026delinsCCA ENSP00000514759.2:p.Asn342Pro
ENST00000710265.1:c.931_933delinsCCA ENSP00000518161.1:p.Asn311Pro
ENST00000472832.3:c.931_933delinsCCA ENSP00000483066.2:p.Asn311Pro
ENST00000688158.2:n.1666_1668delinsCCA
ENST00000688922.2:c.*761_*763delinsCCA ENSP00000508742.2:n.*761_*763delinsCCA
ENST00000700021.1:c.886_888delinsCCA ENSP00000514757.1:p.Asn296Pro
ENST00000700022.1:c.*270_*272delinsCCA ENSP00000514758.1:n.*270_*272delinsCCA
ENST00000700023.1:n.2089_2091delinsCCA
ENST00000700024.1:n.2323_2325delinsCCA
ENST00000700025.1:n.1700_1702delinsCCA
ENST00000700026.1:n.568_570delinsCCA
ENST00000706954.1:c.931_933delinsCCA ENSP00000516674.1:p.Asn311Pro
ENST00000706955.1:c.*966_*968delinsCCA ENSP00000516675.1:n.*966_*968delinsCCA
ENST00000686459.1:c.*517_*519delinsCCA ENSP00000508909.1:n.*517_*519delinsCCA
ENST00000688158.1:c.*1042_*1044delinsCCA ENSP00000509254.1:n.*1042_*1044delinsCCA
ENST00000688308.1:c.931_933delinsCCA ENSP00000508752.1:p.Asn311Pro
ENST00000688922.1:c.852_854delinsCCA
ENST00000693560.1:c.1450_1452delinsCCA ENSP00000509861.1:p.Asn484Pro
ENST00000371953.8:c.931_933delinsCCA MANE Select ENSP00000361021.3:p.Asn311Pro
ENST00000371953.7:c.931_933delinsCCA ENSP00000361021.3:p.Asn311Pro
ENST00000472832.2:c.358_360delinsCCA ENSP00000483066.1:p.Asn120Pro
NM_000314.5:c.931_933delinsCCA NP_000305.3:p.Asn311Pro
NM_000314.6:c.931_933delinsCCA NP_000305.3:p.Asn311Pro
NM_001304717.2:c.1450_1452delinsCCA NP_001291646.2:p.Asn484Pro
NM_001304718.1:c.340_342delinsCCA NP_001291647.1:p.Asn114Pro
XM_006717926.2:c.886_888delinsCCA XP_006717989.1:p.Asn296Pro
XM_011539981.1:c.931_933delinsCCA XP_011538283.1:p.Asn311Pro
XM_011539982.1:c.835_837delinsCCA XP_011538284.1:p.Asn279Pro
XR_945791.1:n.1501_1503delinsCCA
NM_000314.7:c.931_933delinsCCA NP_000305.3:p.Asn311Pro
NM_001304717.5:c.1450_1452delinsCCA NP_001291646.4:p.Asn484Pro
NM_001304718.2:c.340_342delinsCCA NP_001291647.1:p.Asn114Pro
NM_000314.8:c.931_933delinsCCA MANE Select NP_000305.3:p.Asn311Pro