Canonical Allele Identifier: CA891837208
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965326_87965327delinsTC , CM000672.2:g.87965326_87965327delinsTC GRCh38
NC_000010.10:g.89725083_89725084delinsTC , CM000672.1:g.89725083_89725084delinsTC GRCh37
NC_000010.9:g.89715063_89715064delinsTC NCBI36
NG_007466.2:g.106888_106889delinsTC , LRG_311:g.106888_106889delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1159_1160delinsTC ENSP00000514759.2:p.Asn387Ser
ENST00000710265.1:c.*95_*96delinsTC ENSP00000518161.1:n.*95_*96delinsTC
ENST00000688158.2:n.1801_1802delinsTC
ENST00000688922.2:c.*896_*897delinsTC ENSP00000508742.2:n.*896_*897delinsTC
ENST00000700021.1:c.1021_1022delinsTC ENSP00000514757.1:p.Asn341Ser
ENST00000700022.1:c.*405_*406delinsTC ENSP00000514758.1:n.*405_*406delinsTC
ENST00000700023.1:n.2224_2225delinsTC
ENST00000700024.1:n.2458_2459delinsTC
ENST00000706954.1:c.1066_1067delinsTC ENSP00000516674.1:p.Asn356Ser
ENST00000706955.1:c.*1101_*1102delinsTC ENSP00000516675.1:n.*1101_*1102delinsTC
ENST00000686459.1:c.*652_*653delinsTC ENSP00000508909.1:n.*652_*653delinsTC
ENST00000688158.1:c.*1177_*1178delinsTC ENSP00000509254.1:n.*1177_*1178delinsTC
ENST00000688308.1:c.1066_1067delinsTC ENSP00000508752.1:p.Asn356Ser
ENST00000688922.1:c.987_988delinsTC
ENST00000693560.1:c.1585_1586delinsTC ENSP00000509861.1:p.Asn529Ser
ENST00000371953.8:c.1066_1067delinsTC MANE Select ENSP00000361021.3:p.Asn356Ser
ENST00000371953.7:c.1066_1067delinsTC ENSP00000361021.3:p.Asn356Ser
NM_000314.5:c.1066_1067delinsTC NP_000305.3:p.Asn356Ser
NM_000314.6:c.1066_1067delinsTC NP_000305.3:p.Asn356Ser
NM_001304717.2:c.1585_1586delinsTC NP_001291646.2:p.Asn529Ser
NM_001304718.1:c.475_476delinsTC NP_001291647.1:p.Asn159Ser
XM_006717926.2:c.1021_1022delinsTC XP_006717989.1:p.Asn341Ser
XM_011539982.1:c.970_971delinsTC XP_011538284.1:p.Asn324Ser
XR_945791.1:n.1636_1637delinsTC
NM_000314.7:c.1066_1067delinsTC NP_000305.3:p.Asn356Ser
NM_001304717.5:c.1585_1586delinsTC NP_001291646.4:p.Asn529Ser
NM_001304718.2:c.475_476delinsTC NP_001291647.1:p.Asn159Ser
NM_000314.8:c.1066_1067delinsTC MANE Select NP_000305.3:p.Asn356Ser