Canonical Allele Identifier: CA891841239
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961020_87961021delinsCT , CM000672.2:g.87961020_87961021delinsCT GRCh38
NC_000010.10:g.89720777_89720778delinsCT , CM000672.1:g.89720777_89720778delinsCT GRCh37
NC_000010.9:g.89710757_89710758delinsCT NCBI36
NG_007466.2:g.102582_102583delinsCT , LRG_311:g.102582_102583delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1021_1022delinsCT ENSP00000514759.2:p.Asp341Leu
ENST00000710265.1:c.928_929delinsCT ENSP00000518161.1:p.Asp310Leu
ENST00000472832.3:c.928_929delinsCT ENSP00000483066.2:p.Asp310Leu
ENST00000688158.2:n.1663_1664delinsCT
ENST00000688922.2:c.*758_*759delinsCT ENSP00000508742.2:n.*758_*759delinsCT
ENST00000700021.1:c.883_884delinsCT ENSP00000514757.1:p.Asp295Leu
ENST00000700022.1:c.*267_*268delinsCT ENSP00000514758.1:n.*267_*268delinsCT
ENST00000700023.1:n.2086_2087delinsCT
ENST00000700024.1:n.2320_2321delinsCT
ENST00000700025.1:n.1697_1698delinsCT
ENST00000700026.1:n.565_566delinsCT
ENST00000706954.1:c.928_929delinsCT ENSP00000516674.1:p.Asp310Leu
ENST00000706955.1:c.*963_*964delinsCT ENSP00000516675.1:n.*963_*964delinsCT
ENST00000686459.1:c.*514_*515delinsCT ENSP00000508909.1:n.*514_*515delinsCT
ENST00000688158.1:c.*1039_*1040delinsCT ENSP00000509254.1:n.*1039_*1040delinsCT
ENST00000688308.1:c.928_929delinsCT ENSP00000508752.1:p.Asp310Leu
ENST00000688922.1:c.849_850delinsCT
ENST00000693560.1:c.1447_1448delinsCT ENSP00000509861.1:p.Asp483Leu
ENST00000371953.8:c.928_929delinsCT MANE Select ENSP00000361021.3:p.Asp310Leu
ENST00000371953.7:c.928_929delinsCT ENSP00000361021.3:p.Asp310Leu
ENST00000472832.2:c.355_356delinsCT ENSP00000483066.1:p.Asp119Leu
NM_000314.5:c.928_929delinsCT NP_000305.3:p.Asp310Leu
NM_000314.6:c.928_929delinsCT NP_000305.3:p.Asp310Leu
NM_001304717.2:c.1447_1448delinsCT NP_001291646.2:p.Asp483Leu
NM_001304718.1:c.337_338delinsCT NP_001291647.1:p.Asp113Leu
XM_006717926.2:c.883_884delinsCT XP_006717989.1:p.Asp295Leu
XM_011539981.1:c.928_929delinsCT XP_011538283.1:p.Asp310Leu
XM_011539982.1:c.832_833delinsCT XP_011538284.1:p.Asp278Leu
XR_945791.1:n.1498_1499delinsCT
NM_000314.7:c.928_929delinsCT NP_000305.3:p.Asp310Leu
NM_001304717.5:c.1447_1448delinsCT NP_001291646.4:p.Asp483Leu
NM_001304718.2:c.337_338delinsCT NP_001291647.1:p.Asp113Leu
NM_000314.8:c.928_929delinsCT MANE Select NP_000305.3:p.Asp310Leu