Canonical Allele Identifier: CA891837834
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965395_87965396delinsGT , CM000672.2:g.87965395_87965396delinsGT GRCh38
NC_000010.10:g.89725152_89725153delinsGT , CM000672.1:g.89725152_89725153delinsGT GRCh37
NC_000010.9:g.89715132_89715133delinsGT NCBI36
NG_007466.2:g.106957_106958delinsGT , LRG_311:g.106957_106958delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1228_1229delinsGT ENSP00000514759.2:p.Tyr410Val
ENST00000710265.1:c.*164_*165delinsGT ENSP00000518161.1:n.*164_*165delinsGT
ENST00000688158.2:n.1870_1871delinsGT
ENST00000688922.2:c.*965_*966delinsGT ENSP00000508742.2:n.*965_*966delinsGT
ENST00000700021.1:c.1090_1091delinsGT ENSP00000514757.1:p.Tyr364Val
ENST00000700022.1:c.*474_*475delinsGT ENSP00000514758.1:n.*474_*475delinsGT
ENST00000700023.1:n.2293_2294delinsGT
ENST00000700024.1:n.2527_2528delinsGT
ENST00000706954.1:c.1135_1136delinsGT ENSP00000516674.1:p.Tyr379Val
ENST00000706955.1:c.*1170_*1171delinsGT ENSP00000516675.1:n.*1170_*1171delinsGT
ENST00000686459.1:c.*721_*722delinsGT ENSP00000508909.1:n.*721_*722delinsGT
ENST00000688158.1:c.*1246_*1247delinsGT ENSP00000509254.1:n.*1246_*1247delinsGT
ENST00000688308.1:c.1135_1136delinsGT ENSP00000508752.1:p.Tyr379Val
ENST00000688922.1:c.1056_1057delinsGT
ENST00000693560.1:c.1654_1655delinsGT ENSP00000509861.1:p.Tyr552Val
ENST00000371953.8:c.1135_1136delinsGT MANE Select ENSP00000361021.3:p.Tyr379Val
ENST00000371953.7:c.1135_1136delinsGT ENSP00000361021.3:p.Tyr379Val
NM_000314.5:c.1135_1136delinsGT NP_000305.3:p.Tyr379Val
NM_000314.6:c.1135_1136delinsGT NP_000305.3:p.Tyr379Val
NM_001304717.2:c.1654_1655delinsGT NP_001291646.2:p.Tyr552Val
NM_001304718.1:c.544_545delinsGT NP_001291647.1:p.Tyr182Val
XM_006717926.2:c.1090_1091delinsGT XP_006717989.1:p.Tyr364Val
XM_011539982.1:c.1039_1040delinsGT XP_011538284.1:p.Tyr347Val
XR_945791.1:n.1705_1706delinsGT
NM_000314.7:c.1135_1136delinsGT NP_000305.3:p.Tyr379Val
NM_001304717.5:c.1654_1655delinsGT NP_001291646.4:p.Tyr552Val
NM_001304718.2:c.544_545delinsGT NP_001291647.1:p.Tyr182Val
NM_000314.8:c.1135_1136delinsGT MANE Select NP_000305.3:p.Tyr379Val