Canonical Allele Identifier: CA891837835
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965395_87965396delinsAC , CM000672.2:g.87965395_87965396delinsAC GRCh38
NC_000010.10:g.89725152_89725153delinsAC , CM000672.1:g.89725152_89725153delinsAC GRCh37
NC_000010.9:g.89715132_89715133delinsAC NCBI36
NG_007466.2:g.106957_106958delinsAC , LRG_311:g.106957_106958delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1228_1229delinsAC ENSP00000514759.2:p.Tyr410Thr
ENST00000710265.1:c.*164_*165delinsAC ENSP00000518161.1:n.*164_*165delinsAC
ENST00000688158.2:n.1870_1871delinsAC
ENST00000688922.2:c.*965_*966delinsAC ENSP00000508742.2:n.*965_*966delinsAC
ENST00000700021.1:c.1090_1091delinsAC ENSP00000514757.1:p.Tyr364Thr
ENST00000700022.1:c.*474_*475delinsAC ENSP00000514758.1:n.*474_*475delinsAC
ENST00000700023.1:n.2293_2294delinsAC
ENST00000700024.1:n.2527_2528delinsAC
ENST00000706954.1:c.1135_1136delinsAC ENSP00000516674.1:p.Tyr379Thr
ENST00000706955.1:c.*1170_*1171delinsAC ENSP00000516675.1:n.*1170_*1171delinsAC
ENST00000686459.1:c.*721_*722delinsAC ENSP00000508909.1:n.*721_*722delinsAC
ENST00000688158.1:c.*1246_*1247delinsAC ENSP00000509254.1:n.*1246_*1247delinsAC
ENST00000688308.1:c.1135_1136delinsAC ENSP00000508752.1:p.Tyr379Thr
ENST00000688922.1:c.1056_1057delinsAC
ENST00000693560.1:c.1654_1655delinsAC ENSP00000509861.1:p.Tyr552Thr
ENST00000371953.8:c.1135_1136delinsAC MANE Select ENSP00000361021.3:p.Tyr379Thr
ENST00000371953.7:c.1135_1136delinsAC ENSP00000361021.3:p.Tyr379Thr
NM_000314.5:c.1135_1136delinsAC NP_000305.3:p.Tyr379Thr
NM_000314.6:c.1135_1136delinsAC NP_000305.3:p.Tyr379Thr
NM_001304717.2:c.1654_1655delinsAC NP_001291646.2:p.Tyr552Thr
NM_001304718.1:c.544_545delinsAC NP_001291647.1:p.Tyr182Thr
XM_006717926.2:c.1090_1091delinsAC XP_006717989.1:p.Tyr364Thr
XM_011539982.1:c.1039_1040delinsAC XP_011538284.1:p.Tyr347Thr
XR_945791.1:n.1705_1706delinsAC
NM_000314.7:c.1135_1136delinsAC NP_000305.3:p.Tyr379Thr
NM_001304717.5:c.1654_1655delinsAC NP_001291646.4:p.Tyr552Thr
NM_001304718.2:c.544_545delinsAC NP_001291647.1:p.Tyr182Thr
NM_000314.8:c.1135_1136delinsAC MANE Select NP_000305.3:p.Tyr379Thr