Canonical Allele Identifier: CA891840676
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864543_87864544delinsAT , CM000672.2:g.87864543_87864544delinsAT GRCh38
NC_000010.10:g.89624300_89624301delinsAT , CM000672.1:g.89624300_89624301delinsAT GRCh37
NC_000010.9:g.89614280_89614281delinsAT NCBI36
NG_007466.2:g.6105_6106delinsAT , LRG_311:g.6105_6106delinsAT
NG_033079.1:g.3894_3895delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.74_75delinsAT ENSP00000514759.2:p.Leu25Tyr
ENST00000710265.1:c.74_75delinsAT ENSP00000518161.1:p.Leu25Tyr
ENST00000472832.3:c.74_75delinsAT ENSP00000483066.2:p.Leu25Tyr
ENST00000688922.2:c.74_75delinsAT ENSP00000508742.2:p.Leu25Tyr
ENST00000700021.1:c.74_75delinsAT ENSP00000514757.1:p.Leu25Tyr
ENST00000700022.1:c.74_75delinsAT ENSP00000514758.1:p.Leu25Tyr
ENST00000706954.1:c.74_75delinsAT ENSP00000516674.1:p.Leu25Tyr
ENST00000706955.1:c.74_75delinsAT ENSP00000516675.1:p.Leu25Tyr
ENST00000686459.1:c.74_75delinsAT ENSP00000508909.1:p.Leu25Tyr
ENST00000688158.1:c.74_75delinsAT ENSP00000509254.1:p.Leu25Tyr
ENST00000688308.1:c.74_75delinsAT ENSP00000508752.1:p.Leu25Tyr
ENST00000693560.1:c.593_594delinsAT ENSP00000509861.1:p.Leu198Tyr
ENST00000371953.8:c.74_75delinsAT MANE Select ENSP00000361021.3:p.Leu25Tyr
ENST00000371953.7:c.74_75delinsAT ENSP00000361021.3:p.Leu25Tyr
ENST00000462694.1:n.76_77delinsAT
ENST00000487939.1:n.95_96delinsAT
ENST00000610634.1:c.-29_-28delinsAT ENSP00000477517.1:n.-29_-28delinsAT
ENST00000618586.1:n.43_44delinsAT
NM_000314.5:c.74_75delinsAT NP_000305.3:p.Leu25Tyr
NM_000314.6:c.74_75delinsAT NP_000305.3:p.Leu25Tyr
NM_001304717.2:c.593_594delinsAT NP_001291646.2:p.Leu198Tyr
NM_001304718.1:c.-632_-631delinsAT NP_001291647.1:n.-632_-631delinsAT
XM_006717926.2:c.74_75delinsAT XP_006717989.1:p.Leu25Tyr
XM_011539981.1:c.74_75delinsAT XP_011538283.1:p.Leu25Tyr
XR_945789.1:n.786_787delinsAT
XR_945790.1:n.786_787delinsAT
XR_945791.1:n.786_787delinsAT
NM_000314.7:c.74_75delinsAT NP_000305.3:p.Leu25Tyr
NM_001304717.5:c.593_594delinsAT NP_001291646.4:p.Leu198Tyr
NM_001304718.2:c.-632_-631delinsAT NP_001291647.1:n.-632_-631delinsAT
NM_000314.8:c.74_75delinsAT MANE Select NP_000305.3:p.Leu25Tyr