Canonical Allele Identifier: CA891839858
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957960_87957962delinsATG , CM000672.2:g.87957960_87957962delinsATG GRCh38
NC_000010.10:g.89717717_89717719delinsATG , CM000672.1:g.89717717_89717719delinsATG GRCh37
NC_000010.9:g.89707697_89707699delinsATG NCBI36
NG_007466.2:g.99522_99524delinsATG , LRG_311:g.99522_99524delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.742_744delinsATG ENSP00000514759.2:p.Pro248Met
ENST00000710265.1:c.742_744delinsATG ENSP00000518161.1:p.Pro248Met
ENST00000472832.3:c.742_744delinsATG ENSP00000483066.2:p.Pro248Met
ENST00000688158.2:n.1477_1479delinsATG
ENST00000688922.2:c.*572_*574delinsATG ENSP00000508742.2:n.*572_*574delinsATG
ENST00000700021.1:c.697_699delinsATG ENSP00000514757.1:p.Pro233Met
ENST00000700022.1:c.*81_*83delinsATG ENSP00000514758.1:n.*81_*83delinsATG
ENST00000700023.1:n.1900_1902delinsATG
ENST00000700024.1:n.2134_2136delinsATG
ENST00000700025.1:n.1511_1513delinsATG
ENST00000700026.1:n.379_381delinsATG
ENST00000700029.1:c.576_578delinsATG
ENST00000706954.1:c.742_744delinsATG ENSP00000516674.1:p.Pro248Met
ENST00000706955.1:c.*777_*779delinsATG ENSP00000516675.1:n.*777_*779delinsATG
ENST00000686459.1:c.*328_*330delinsATG ENSP00000508909.1:n.*328_*330delinsATG
ENST00000688158.1:c.*853_*855delinsATG ENSP00000509254.1:n.*853_*855delinsATG
ENST00000688308.1:c.742_744delinsATG ENSP00000508752.1:p.Pro248Met
ENST00000688922.1:c.663_665delinsATG
ENST00000693560.1:c.1261_1263delinsATG ENSP00000509861.1:p.Pro421Met
ENST00000371953.8:c.742_744delinsATG MANE Select ENSP00000361021.3:p.Pro248Met
ENST00000371953.7:c.742_744delinsATG ENSP00000361021.3:p.Pro248Met
ENST00000472832.2:c.169_171delinsATG ENSP00000483066.1:p.Pro57Met
NM_000314.5:c.742_744delinsATG NP_000305.3:p.Pro248Met
NM_000314.6:c.742_744delinsATG NP_000305.3:p.Pro248Met
NM_001304717.2:c.1261_1263delinsATG NP_001291646.2:p.Pro421Met
NM_001304718.1:c.151_153delinsATG NP_001291647.1:p.Pro51Met
XM_006717926.2:c.697_699delinsATG XP_006717989.1:p.Pro233Met
XM_011539981.1:c.742_744delinsATG XP_011538283.1:p.Pro248Met
XM_011539982.1:c.646_648delinsATG XP_011538284.1:p.Pro216Met
XR_945791.1:n.1312_1314delinsATG
NM_000314.7:c.742_744delinsATG NP_000305.3:p.Pro248Met
NM_001304717.5:c.1261_1263delinsATG NP_001291646.4:p.Pro421Met
NM_001304718.2:c.151_153delinsATG NP_001291647.1:p.Pro51Met
NM_000314.8:c.742_744delinsATG MANE Select NP_000305.3:p.Pro248Met