Canonical Allele Identifier: CA891841612
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965371_87965372delinsTC , CM000672.2:g.87965371_87965372delinsTC GRCh38
NC_000010.10:g.89725128_89725129delinsTC , CM000672.1:g.89725128_89725129delinsTC GRCh37
NC_000010.9:g.89715108_89715109delinsTC NCBI36
NG_007466.2:g.106933_106934delinsTC , LRG_311:g.106933_106934delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1204_1205delinsTC ENSP00000514759.2:p.Asp402Ser
ENST00000710265.1:c.*140_*141delinsTC ENSP00000518161.1:n.*140_*141delinsTC
ENST00000688158.2:n.1846_1847delinsTC
ENST00000688922.2:c.*941_*942delinsTC ENSP00000508742.2:n.*941_*942delinsTC
ENST00000700021.1:c.1066_1067delinsTC ENSP00000514757.1:p.Asp356Ser
ENST00000700022.1:c.*450_*451delinsTC ENSP00000514758.1:n.*450_*451delinsTC
ENST00000700023.1:n.2269_2270delinsTC
ENST00000700024.1:n.2503_2504delinsTC
ENST00000706954.1:c.1111_1112delinsTC ENSP00000516674.1:p.Asp371Ser
ENST00000706955.1:c.*1146_*1147delinsTC ENSP00000516675.1:n.*1146_*1147delinsTC
ENST00000686459.1:c.*697_*698delinsTC ENSP00000508909.1:n.*697_*698delinsTC
ENST00000688158.1:c.*1222_*1223delinsTC ENSP00000509254.1:n.*1222_*1223delinsTC
ENST00000688308.1:c.1111_1112delinsTC ENSP00000508752.1:p.Asp371Ser
ENST00000688922.1:c.1032_1033delinsTC
ENST00000693560.1:c.1630_1631delinsTC ENSP00000509861.1:p.Asp544Ser
ENST00000371953.8:c.1111_1112delinsTC MANE Select ENSP00000361021.3:p.Asp371Ser
ENST00000371953.7:c.1111_1112delinsTC ENSP00000361021.3:p.Asp371Ser
NM_000314.5:c.1111_1112delinsTC NP_000305.3:p.Asp371Ser
NM_000314.6:c.1111_1112delinsTC NP_000305.3:p.Asp371Ser
NM_001304717.2:c.1630_1631delinsTC NP_001291646.2:p.Asp544Ser
NM_001304718.1:c.520_521delinsTC NP_001291647.1:p.Asp174Ser
XM_006717926.2:c.1066_1067delinsTC XP_006717989.1:p.Asp356Ser
XM_011539982.1:c.1015_1016delinsTC XP_011538284.1:p.Asp339Ser
XR_945791.1:n.1681_1682delinsTC
NM_000314.7:c.1111_1112delinsTC NP_000305.3:p.Asp371Ser
NM_001304717.5:c.1630_1631delinsTC NP_001291646.4:p.Asp544Ser
NM_001304718.2:c.520_521delinsTC NP_001291647.1:p.Asp174Ser
NM_000314.8:c.1111_1112delinsTC MANE Select NP_000305.3:p.Asp371Ser