Canonical Allele Identifier: CA891835208
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87925550_87925552delinsAAT , CM000672.2:g.87925550_87925552delinsAAT GRCh38
NC_000010.10:g.89685307_89685309delinsAAT , CM000672.1:g.89685307_89685309delinsAAT GRCh37
NC_000010.9:g.89675287_89675289delinsAAT NCBI36
NG_007466.2:g.67112_67114delinsAAT , LRG_311:g.67112_67114delinsAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.202_204delinsAAT ENSP00000514759.2:p.Tyr68Asn
ENST00000710265.1:c.202_204delinsAAT ENSP00000518161.1:p.Tyr68Asn
ENST00000472832.3:c.202_204delinsAAT ENSP00000483066.2:p.Tyr68Asn
ENST00000688158.2:n.937_939delinsAAT
ENST00000688922.2:c.202_204delinsAAT ENSP00000508742.2:p.Tyr68Asn
ENST00000700021.1:c.165-5496_165-5494delinsAAT ENSP00000514757.1:n.165-5496_165-5494delinsAAT
ENST00000700022.1:c.202_204delinsAAT ENSP00000514758.1:p.Tyr68Asn
ENST00000700029.1:c.36_38delinsAAT
ENST00000706954.1:c.202_204delinsAAT ENSP00000516674.1:p.Tyr68Asn
ENST00000706955.1:c.*237_*239delinsAAT ENSP00000516675.1:n.*237_*239delinsAAT
ENST00000686459.1:c.202_204delinsAAT ENSP00000508909.1:p.Tyr68Asn
ENST00000688158.1:c.*313_*315delinsAAT ENSP00000509254.1:n.*313_*315delinsAAT
ENST00000688308.1:c.202_204delinsAAT ENSP00000508752.1:p.Tyr68Asn
ENST00000688922.1:c.71_73delinsAAT
ENST00000693560.1:c.721_723delinsAAT ENSP00000509861.1:p.Tyr241Asn
ENST00000371953.8:c.202_204delinsAAT MANE Select ENSP00000361021.3:p.Tyr68Asn
ENST00000371953.7:c.202_204delinsAAT ENSP00000361021.3:p.Tyr68Asn
ENST00000498703.1:n.28_30delinsAAT
ENST00000610634.1:c.100_102delinsAAT ENSP00000477517.1:p.Tyr34Asn
NM_000314.5:c.202_204delinsAAT NP_000305.3:p.Tyr68Asn
NM_000314.6:c.202_204delinsAAT NP_000305.3:p.Tyr68Asn
NM_001304717.2:c.721_723delinsAAT NP_001291646.2:p.Tyr241Asn
NM_001304718.1:c.-541-5496_-541-5494delinsAAT NP_001291647.1:n.-541-5496_-541-5494delinsAAT
XM_006717926.2:c.165-5496_165-5494delinsAAT XP_006717989.1:n.165-5496_165-5494delinsAAT
XM_011539981.1:c.202_204delinsAAT XP_011538283.1:p.Tyr68Asn
XM_011539982.1:c.106_108delinsAAT XP_011538284.1:p.Tyr36Asn
XR_945789.1:n.914_916delinsAAT
XR_945790.1:n.914_916delinsAAT
XR_945791.1:n.914_916delinsAAT
NM_000314.7:c.202_204delinsAAT NP_000305.3:p.Tyr68Asn
NM_001304717.5:c.721_723delinsAAT NP_001291646.4:p.Tyr241Asn
NM_001304718.2:c.-541-5496_-541-5494delinsAAT NP_001291647.1:n.-541-5496_-541-5494delinsAAT
NM_000314.8:c.202_204delinsAAT MANE Select NP_000305.3:p.Tyr68Asn