Canonical Allele Identifier: CA891834627
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894045_87894046delinsAA , CM000672.2:g.87894045_87894046delinsAA GRCh38
NC_000010.10:g.89653802_89653803delinsAA , CM000672.1:g.89653802_89653803delinsAA GRCh37
NC_000010.9:g.89643782_89643783delinsAA NCBI36
NG_007466.2:g.35607_35608delinsAA , LRG_311:g.35607_35608delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.100_101delinsAA ENSP00000514759.2:p.Ala34Asn
ENST00000710265.1:c.100_101delinsAA ENSP00000518161.1:p.Ala34Asn
ENST00000472832.3:c.100_101delinsAA ENSP00000483066.2:p.Ala34Asn
ENST00000688158.2:n.899+13607_899+13608delinsAA
ENST00000688922.2:c.100_101delinsAA ENSP00000508742.2:p.Ala34Asn
ENST00000700021.1:c.100_101delinsAA ENSP00000514757.1:p.Ala34Asn
ENST00000700022.1:c.100_101delinsAA ENSP00000514758.1:p.Ala34Asn
ENST00000706954.1:c.100_101delinsAA ENSP00000516674.1:p.Ala34Asn
ENST00000706955.1:c.*135_*136delinsAA ENSP00000516675.1:n.*135_*136delinsAA
ENST00000686459.1:c.100_101delinsAA ENSP00000508909.1:p.Ala34Asn
ENST00000688158.1:c.*275+13607_*275+13608delinsAA ENSP00000509254.1:n.*275+13607_*275+13608delinsAA
ENST00000688308.1:c.100_101delinsAA ENSP00000508752.1:p.Ala34Asn
ENST00000693560.1:c.619_620delinsAA ENSP00000509861.1:p.Ala207Asn
ENST00000371953.8:c.100_101delinsAA MANE Select ENSP00000361021.3:p.Ala34Asn
ENST00000371953.7:c.100_101delinsAA ENSP00000361021.3:p.Ala34Asn
ENST00000462694.1:n.102_103delinsAA
ENST00000610634.1:c.-3_-2delinsAA ENSP00000477517.1:n.-3_-2delinsAA
NM_000314.5:c.100_101delinsAA NP_000305.3:p.Ala34Asn
NM_000314.6:c.100_101delinsAA NP_000305.3:p.Ala34Asn
NM_001304717.2:c.619_620delinsAA NP_001291646.2:p.Ala207Asn
NM_001304718.1:c.-606_-605delinsAA NP_001291647.1:n.-606_-605delinsAA
XM_006717926.2:c.100_101delinsAA XP_006717989.1:p.Ala34Asn
XM_011539981.1:c.100_101delinsAA XP_011538283.1:p.Ala34Asn
XM_011539982.1:c.68+13607_68+13608delinsAA XP_011538284.1:n.68+13607_68+13608delinsAA
XR_945789.1:n.812_813delinsAA
XR_945790.1:n.812_813delinsAA
XR_945791.1:n.812_813delinsAA
NM_000314.7:c.100_101delinsAA NP_000305.3:p.Ala34Asn
NM_001304717.5:c.619_620delinsAA NP_001291646.4:p.Ala207Asn
NM_001304718.2:c.-606_-605delinsAA NP_001291647.1:n.-606_-605delinsAA
NM_000314.8:c.100_101delinsAA MANE Select NP_000305.3:p.Ala34Asn