Canonical Allele Identifier: CA2579926449
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965341_87965342delinsTC , CM000672.2:g.87965341_87965342delinsTC GRCh38
NC_000010.10:g.89725098_89725099delinsTC , CM000672.1:g.89725098_89725099delinsTC GRCh37
NC_000010.9:g.89715078_89715079delinsTC NCBI36
NG_007466.2:g.106903_106904delinsTC , LRG_311:g.106903_106904delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1174_1175delinsTC ENSP00000514759.2:p.Ser392=
ENST00000710265.1:c.*110_*111delinsTC ENSP00000518161.1:n.*110_*111delinsTC
ENST00000688158.2:n.1816_1817delinsTC
ENST00000688922.2:c.*911_*912delinsTC ENSP00000508742.2:n.*911_*912delinsTC
ENST00000700021.1:c.1036_1037delinsTC ENSP00000514757.1:p.Ser346=
ENST00000700022.1:c.*420_*421delinsTC ENSP00000514758.1:n.*420_*421delinsTC
ENST00000700023.1:n.2239_2240delinsTC
ENST00000700024.1:n.2473_2474delinsTC
ENST00000706954.1:c.1081_1082delinsTC ENSP00000516674.1:p.Ser361=
ENST00000706955.1:c.*1116_*1117delinsTC ENSP00000516675.1:n.*1116_*1117delinsTC
ENST00000686459.1:c.*667_*668delinsTC ENSP00000508909.1:n.*667_*668delinsTC
ENST00000688158.1:c.*1192_*1193delinsTC ENSP00000509254.1:n.*1192_*1193delinsTC
ENST00000688308.1:c.1081_1082delinsTC ENSP00000508752.1:p.Ser361=
ENST00000688922.1:c.1002_1003delinsTC
ENST00000693560.1:c.1600_1601delinsTC ENSP00000509861.1:p.Ser534=
ENST00000371953.8:c.1081_1082delinsTC MANE Select ENSP00000361021.3:p.Ser361=
ENST00000371953.7:c.1081_1082delinsTC ENSP00000361021.3:p.Ser361=
NM_000314.5:c.1081_1082delinsTC NP_000305.3:p.Ser361=
NM_000314.6:c.1081_1082delinsTC NP_000305.3:p.Ser361=
NM_001304717.2:c.1600_1601delinsTC NP_001291646.2:p.Ser534=
NM_001304718.1:c.490_491delinsTC NP_001291647.1:p.Ser164=
XM_006717926.2:c.1036_1037delinsTC XP_006717989.1:p.Ser346=
XM_011539982.1:c.985_986delinsTC XP_011538284.1:p.Ser329=
XR_945791.1:n.1651_1652delinsTC
NM_000314.7:c.1081_1082delinsTC NP_000305.3:p.Ser361=
NM_001304717.5:c.1600_1601delinsTC NP_001291646.4:p.Ser534=
NM_001304718.2:c.490_491delinsTC NP_001291647.1:p.Ser164=
NM_000314.8:c.1081_1082delinsTC MANE Select NP_000305.3:p.Ser361=