Canonical Allele Identifier: CA1926173918
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965373_87965377delinsCAATG , CM000672.2:g.87965373_87965377delinsCAATG GRCh38
NC_000010.10:g.89725130_89725134delinsCAATG , CM000672.1:g.89725130_89725134delinsCAATG GRCh37
NC_000010.9:g.89715110_89715114delinsCAATG NCBI36
NG_007466.2:g.106935_106939delinsCAATG , LRG_311:g.106935_106939delinsCAATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1206_1210delinsCAATG ENSP00000514759.2:p.Asp402=
ENST00000710265.1:c.*142_*146delinsCAATG ENSP00000518161.1:n.*142_*146delinsCAATG
ENST00000688158.2:n.1848_1852delinsCAATG
ENST00000688922.2:c.*943_*947delinsCAATG ENSP00000508742.2:n.*943_*947delinsCAATG
ENST00000700021.1:c.1068_1072delinsCAATG ENSP00000514757.1:p.Asp356=
ENST00000700022.1:c.*452_*456delinsCAATG ENSP00000514758.1:n.*452_*456delinsCAATG
ENST00000700023.1:n.2271_2275delinsCAATG
ENST00000700024.1:n.2505_2509delinsCAATG
ENST00000706954.1:c.1113_1117delinsCAATG ENSP00000516674.1:p.Asp371=
ENST00000706955.1:c.*1148_*1152delinsCAATG ENSP00000516675.1:n.*1148_*1152delinsCAATG
ENST00000686459.1:c.*699_*703delinsCAATG ENSP00000508909.1:n.*699_*703delinsCAATG
ENST00000688158.1:c.*1224_*1228delinsCAATG ENSP00000509254.1:n.*1224_*1228delinsCAATG
ENST00000688308.1:c.1113_1117delinsCAATG ENSP00000508752.1:p.Asp371=
ENST00000688922.1:c.1034_1038delinsCAATG
ENST00000693560.1:c.1632_1636delinsCAATG ENSP00000509861.1:p.Asp544=
ENST00000371953.8:c.1113_1117delinsCAATG MANE Select ENSP00000361021.3:p.Asp371=
ENST00000371953.7:c.1113_1117delinsCAATG ENSP00000361021.3:p.Asp371=
NM_000314.5:c.1113_1117delinsCAATG NP_000305.3:p.Asp371=
NM_000314.6:c.1113_1117delinsCAATG NP_000305.3:p.Asp371=
NM_001304717.2:c.1632_1636delinsCAATG NP_001291646.2:p.Asp544=
NM_001304718.1:c.522_526delinsCAATG NP_001291647.1:p.Asp174=
XM_006717926.2:c.1068_1072delinsCAATG XP_006717989.1:p.Asp356=
XM_011539982.1:c.1017_1021delinsCAATG XP_011538284.1:p.Asp339=
XR_945791.1:n.1683_1687delinsCAATG
NM_000314.7:c.1113_1117delinsCAATG NP_000305.3:p.Asp371=
NM_001304717.5:c.1632_1636delinsCAATG NP_001291646.4:p.Asp544=
NM_001304718.2:c.522_526delinsCAATG NP_001291647.1:p.Asp174=
NM_000314.8:c.1113_1117delinsCAATG MANE Select NP_000305.3:p.Asp371=