Canonical Allele Identifier: CA2610047506
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958163_87958164insACCAG , CM000672.2:g.87958163_87958164insACCAG GRCh38
NC_000010.10:g.89717920_89717921insACCAG , CM000672.1:g.89717920_89717921insACCAG GRCh37
NC_000010.9:g.89707900_89707901insACCAG NCBI36
NG_007466.2:g.99725_99726insACCAG , LRG_311:g.99725_99726insACCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.801+144_801+145insACCAG ENSP00000514759.2:n.801+144_801+145insACCAG
ENST00000710265.1:c.801+144_801+145insACCAG ENSP00000518161.1:n.801+144_801+145insACCAG
ENST00000472832.3:c.801+144_801+145insACCAG ENSP00000483066.2:n.801+144_801+145insACCAG
ENST00000688158.2:n.1536+144_1536+145insACCAG
ENST00000688922.2:c.*631+144_*631+145insACCAG ENSP00000508742.2:n.*631+144_*631+145insACCAG
ENST00000700021.1:c.756+144_756+145insACCAG ENSP00000514757.1:n.756+144_756+145insACCAG
ENST00000700022.1:c.*140+144_*140+145insACCAG ENSP00000514758.1:n.*140+144_*140+145insACCAG
ENST00000700023.1:n.1959+144_1959+145insACCAG
ENST00000700024.1:n.2193+144_2193+145insACCAG
ENST00000700025.1:n.1570+144_1570+145insACCAG
ENST00000700026.1:n.438+144_438+145insACCAG
ENST00000700029.1:c.635+144_635+145insACCAG
ENST00000706954.1:c.801+144_801+145insACCAG ENSP00000516674.1:n.801+144_801+145insACCAG
ENST00000706955.1:c.*836+144_*836+145insACCAG ENSP00000516675.1:n.*836+144_*836+145insACCAG
ENST00000686459.1:c.*387+144_*387+145insACCAG ENSP00000508909.1:n.*387+144_*387+145insACCAG
ENST00000688158.1:c.*912+144_*912+145insACCAG ENSP00000509254.1:n.*912+144_*912+145insACCAG
ENST00000688308.1:c.801+144_801+145insACCAG ENSP00000508752.1:n.801+144_801+145insACCAG
ENST00000688922.1:c.722+144_722+145insACCAG
ENST00000693560.1:c.1320+144_1320+145insACCAG ENSP00000509861.1:n.1320+144_1320+145insACCAG
ENST00000371953.8:c.801+144_801+145insACCAG MANE Select ENSP00000361021.3:n.801+144_801+145insACCAG
ENST00000371953.7:c.801+144_801+145insACCAG ENSP00000361021.3:n.801+144_801+145insACCAG
ENST00000472832.2:c.228+144_228+145insACCAG ENSP00000483066.1:n.228+144_228+145insACCAG
NM_000314.5:c.801+144_801+145insACCAG NP_000305.3:n.801+144_801+145insACCAG
NM_000314.6:c.801+144_801+145insACCAG NP_000305.3:n.801+144_801+145insACCAG
NM_001304717.2:c.1320+144_1320+145insACCAG NP_001291646.2:n.1320+144_1320+145insACCAG
NM_001304718.1:c.210+144_210+145insACCAG NP_001291647.1:n.210+144_210+145insACCAG
XM_006717926.2:c.756+144_756+145insACCAG XP_006717989.1:n.756+144_756+145insACCAG
XM_011539981.1:c.801+144_801+145insACCAG XP_011538283.1:n.801+144_801+145insACCAG
XM_011539982.1:c.705+144_705+145insACCAG XP_011538284.1:n.705+144_705+145insACCAG
XR_945791.1:n.1371+144_1371+145insACCAG
NM_000314.7:c.801+144_801+145insACCAG NP_000305.3:n.801+144_801+145insACCAG
NM_001304717.5:c.1320+144_1320+145insACCAG NP_001291646.4:n.1320+144_1320+145insACCAG
NM_001304718.2:c.210+144_210+145insACCAG NP_001291647.1:n.210+144_210+145insACCAG
NM_000314.8:c.801+144_801+145insACCAG MANE Select NP_000305.3:n.801+144_801+145insACCAG