Canonical Allele Identifier: CA891837761
Community Standard Title: NM_000314.8(PTEN):c.394_395delinsTC (p.Gly132Ser)
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933153_87933154delinsTC , CM000672.2:g.87933153_87933154delinsTC GRCh38
NC_000010.10:g.89692910_89692911delinsTC , CM000672.1:g.89692910_89692911delinsTC GRCh37
NC_000010.9:g.89682890_89682891delinsTC NCBI36
NG_007466.2:g.74715_74716delinsTC , LRG_311:g.74715_74716delinsTC

Transcript Alleles

HGVS Amino-acid Change
NM_000314.8:c.394_395delinsTC MANE Select NP_000305.3:p.Gly132Ser
ENST00000371953.8:c.394_395delinsTC MANE Select ENSP00000361021.3:p.Gly132Ser
NM_000314.5:c.394_395delinsTC NP_000305.3:p.Gly132Ser
NM_000314.6:c.394_395delinsTC NP_000305.3:p.Gly132Ser
NM_000314.7:c.394_395delinsTC NP_000305.3:p.Gly132Ser
NM_001304717.2:c.913_914delinsTC NP_001291646.2:p.Gly305Ser
NM_001304717.5:c.913_914delinsTC NP_001291646.4:p.Gly305Ser
NM_001304718.1:c.-357_-356delinsTC NP_001291647.1:n.-357_-356delinsTC
NM_001304718.2:c.-357_-356delinsTC NP_001291647.1:n.-357_-356delinsTC
ENST00000371953.7:c.394_395delinsTC ENSP00000361021.3:p.Gly132Ser
ENST00000472832.3:c.394_395delinsTC ENSP00000483066.2:p.Gly132Ser
ENST00000498703.1:n.220_221delinsTC
ENST00000610634.1:c.292_293delinsTC ENSP00000477517.1:p.Gly98Ser
ENST00000686459.1:c.394_395delinsTC ENSP00000508909.1:p.Gly132Ser
ENST00000688158.1:c.*505_*506delinsTC ENSP00000509254.1:n.*505_*506delinsTC
ENST00000688158.2:n.1129_1130delinsTC
ENST00000688308.1:c.394_395delinsTC ENSP00000508752.1:p.Gly132Ser
ENST00000688922.1:c.315_316delinsTC
ENST00000688922.2:c.*224_*225delinsTC ENSP00000508742.2:n.*224_*225delinsTC
ENST00000693560.1:c.913_914delinsTC ENSP00000509861.1:p.Gly305Ser
ENST00000700021.1:c.349_350delinsTC ENSP00000514757.1:p.Gly117Ser
ENST00000700022.1:c.394_395delinsTC ENSP00000514758.1:p.Gly132Ser
ENST00000700029.1:c.228_229delinsTC
ENST00000700029.2:c.394_395delinsTC ENSP00000514759.2:p.Gly132Ser
ENST00000706954.1:c.394_395delinsTC ENSP00000516674.1:p.Gly132Ser
ENST00000706955.1:c.*429_*430delinsTC ENSP00000516675.1:n.*429_*430delinsTC
ENST00000710265.1:c.394_395delinsTC ENSP00000518161.1:p.Gly132Ser
XM_006717926.2:c.349_350delinsTC XP_006717989.1:p.Gly117Ser
XM_011539981.1:c.394_395delinsTC XP_011538283.1:p.Gly132Ser
XM_011539982.1:c.298_299delinsTC XP_011538284.1:p.Gly100Ser
XR_945789.1:n.1106_1107delinsTC
XR_945790.1:n.1106_1107delinsTC
XR_945791.1:n.1106_1107delinsTC