Canonical Allele Identifier: CA2579926443
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965351_87965352delinsGG , CM000672.2:g.87965351_87965352delinsGG GRCh38
NC_000010.10:g.89725108_89725109delinsGG , CM000672.1:g.89725108_89725109delinsGG GRCh37
NC_000010.9:g.89715088_89715089delinsGG NCBI36
NG_007466.2:g.106913_106914delinsGG , LRG_311:g.106913_106914delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1184_1185delinsGG ENSP00000514759.2:p.Ser395Trp
ENST00000710265.1:c.*120_*121delinsGG ENSP00000518161.1:n.*120_*121delinsGG
ENST00000688158.2:n.1826_1827delinsGG
ENST00000688922.2:c.*921_*922delinsGG ENSP00000508742.2:n.*921_*922delinsGG
ENST00000700021.1:c.1046_1047delinsGG ENSP00000514757.1:p.Ser349Trp
ENST00000700022.1:c.*430_*431delinsGG ENSP00000514758.1:n.*430_*431delinsGG
ENST00000700023.1:n.2249_2250delinsGG
ENST00000700024.1:n.2483_2484delinsGG
ENST00000706954.1:c.1091_1092delinsGG ENSP00000516674.1:p.Ser364Trp
ENST00000706955.1:c.*1126_*1127delinsGG ENSP00000516675.1:n.*1126_*1127delinsGG
ENST00000686459.1:c.*677_*678delinsGG ENSP00000508909.1:n.*677_*678delinsGG
ENST00000688158.1:c.*1202_*1203delinsGG ENSP00000509254.1:n.*1202_*1203delinsGG
ENST00000688308.1:c.1091_1092delinsGG ENSP00000508752.1:p.Ser364Trp
ENST00000688922.1:c.1012_1013delinsGG
ENST00000693560.1:c.1610_1611delinsGG ENSP00000509861.1:p.Ser537Trp
ENST00000371953.8:c.1091_1092delinsGG MANE Select ENSP00000361021.3:p.Ser364Trp
ENST00000371953.7:c.1091_1092delinsGG ENSP00000361021.3:p.Ser364Trp
NM_000314.5:c.1091_1092delinsGG NP_000305.3:p.Ser364Trp
NM_000314.6:c.1091_1092delinsGG NP_000305.3:p.Ser364Trp
NM_001304717.2:c.1610_1611delinsGG NP_001291646.2:p.Ser537Trp
NM_001304718.1:c.500_501delinsGG NP_001291647.1:p.Ser167Trp
XM_006717926.2:c.1046_1047delinsGG XP_006717989.1:p.Ser349Trp
XM_011539982.1:c.995_996delinsGG XP_011538284.1:p.Ser332Trp
XR_945791.1:n.1661_1662delinsGG
NM_000314.7:c.1091_1092delinsGG NP_000305.3:p.Ser364Trp
NM_001304717.5:c.1610_1611delinsGG NP_001291646.4:p.Ser537Trp
NM_001304718.2:c.500_501delinsGG NP_001291647.1:p.Ser167Trp
NM_000314.8:c.1091_1092delinsGG MANE Select NP_000305.3:p.Ser364Trp