Canonical Allele Identifier: CA891839905
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957969_87957970delinsAT , CM000672.2:g.87957969_87957970delinsAT GRCh38
NC_000010.10:g.89717726_89717727delinsAT , CM000672.1:g.89717726_89717727delinsAT GRCh37
NC_000010.9:g.89707706_89707707delinsAT NCBI36
NG_007466.2:g.99531_99532delinsAT , LRG_311:g.99531_99532delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.751_752delinsAT ENSP00000514759.2:p.Gly251Ile
ENST00000710265.1:c.751_752delinsAT ENSP00000518161.1:p.Gly251Ile
ENST00000472832.3:c.751_752delinsAT ENSP00000483066.2:p.Gly251Ile
ENST00000688158.2:n.1486_1487delinsAT
ENST00000688922.2:c.*581_*582delinsAT ENSP00000508742.2:n.*581_*582delinsAT
ENST00000700021.1:c.706_707delinsAT ENSP00000514757.1:p.Gly236Ile
ENST00000700022.1:c.*90_*91delinsAT ENSP00000514758.1:n.*90_*91delinsAT
ENST00000700023.1:n.1909_1910delinsAT
ENST00000700024.1:n.2143_2144delinsAT
ENST00000700025.1:n.1520_1521delinsAT
ENST00000700026.1:n.388_389delinsAT
ENST00000700029.1:c.585_586delinsAT
ENST00000706954.1:c.751_752delinsAT ENSP00000516674.1:p.Gly251Ile
ENST00000706955.1:c.*786_*787delinsAT ENSP00000516675.1:n.*786_*787delinsAT
ENST00000686459.1:c.*337_*338delinsAT ENSP00000508909.1:n.*337_*338delinsAT
ENST00000688158.1:c.*862_*863delinsAT ENSP00000509254.1:n.*862_*863delinsAT
ENST00000688308.1:c.751_752delinsAT ENSP00000508752.1:p.Gly251Ile
ENST00000688922.1:c.672_673delinsAT
ENST00000693560.1:c.1270_1271delinsAT ENSP00000509861.1:p.Gly424Ile
ENST00000371953.8:c.751_752delinsAT MANE Select ENSP00000361021.3:p.Gly251Ile
ENST00000371953.7:c.751_752delinsAT ENSP00000361021.3:p.Gly251Ile
ENST00000472832.2:c.178_179delinsAT ENSP00000483066.1:p.Gly60Ile
NM_000314.5:c.751_752delinsAT NP_000305.3:p.Gly251Ile
NM_000314.6:c.751_752delinsAT NP_000305.3:p.Gly251Ile
NM_001304717.2:c.1270_1271delinsAT NP_001291646.2:p.Gly424Ile
NM_001304718.1:c.160_161delinsAT NP_001291647.1:p.Gly54Ile
XM_006717926.2:c.706_707delinsAT XP_006717989.1:p.Gly236Ile
XM_011539981.1:c.751_752delinsAT XP_011538283.1:p.Gly251Ile
XM_011539982.1:c.655_656delinsAT XP_011538284.1:p.Gly219Ile
XR_945791.1:n.1321_1322delinsAT
NM_000314.7:c.751_752delinsAT NP_000305.3:p.Gly251Ile
NM_001304717.5:c.1270_1271delinsAT NP_001291646.4:p.Gly424Ile
NM_001304718.2:c.160_161delinsAT NP_001291647.1:p.Gly54Ile
NM_000314.8:c.751_752delinsAT MANE Select NP_000305.3:p.Gly251Ile