Canonical Allele Identifier: CA891836433
Community Standard Title: NM_000314.8(PTEN):c.275_276delinsGT (p.Asp92Gly)
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933034_87933035delinsGT , CM000672.2:g.87933034_87933035delinsGT GRCh38
NC_000010.10:g.89692791_89692792delinsGT , CM000672.1:g.89692791_89692792delinsGT GRCh37
NC_000010.9:g.89682771_89682772delinsGT NCBI36
NG_007466.2:g.74596_74597delinsGT , LRG_311:g.74596_74597delinsGT

Transcript Alleles

HGVS Amino-acid Change
NM_000314.8:c.275_276delinsGT MANE Select NP_000305.3:p.Asp92Gly
ENST00000371953.8:c.275_276delinsGT MANE Select ENSP00000361021.3:p.Asp92Gly
NM_000314.5:c.275_276delinsGT NP_000305.3:p.Asp92Gly
NM_000314.6:c.275_276delinsGT NP_000305.3:p.Asp92Gly
NM_000314.7:c.275_276delinsGT NP_000305.3:p.Asp92Gly
NM_001304717.2:c.794_795delinsGT NP_001291646.2:p.Asp265Gly
NM_001304717.5:c.794_795delinsGT NP_001291646.4:p.Asp265Gly
NM_001304718.1:c.-476_-475delinsGT NP_001291647.1:n.-476_-475delinsGT
NM_001304718.2:c.-476_-475delinsGT NP_001291647.1:n.-476_-475delinsGT
ENST00000371953.7:c.275_276delinsGT ENSP00000361021.3:p.Asp92Gly
ENST00000472832.3:c.275_276delinsGT ENSP00000483066.2:p.Asp92Gly
ENST00000498703.1:n.101_102delinsGT
ENST00000610634.1:c.173_174delinsGT ENSP00000477517.1:p.Asp58Gly
ENST00000686459.1:c.275_276delinsGT ENSP00000508909.1:p.Asp92Gly
ENST00000688158.1:c.*386_*387delinsGT ENSP00000509254.1:n.*386_*387delinsGT
ENST00000688158.2:n.1010_1011delinsGT
ENST00000688308.1:c.275_276delinsGT ENSP00000508752.1:p.Asp92Gly
ENST00000688922.1:c.196_197delinsGT
ENST00000688922.2:c.*105_*106delinsGT ENSP00000508742.2:n.*105_*106delinsGT
ENST00000693560.1:c.794_795delinsGT ENSP00000509861.1:p.Asp265Gly
ENST00000700021.1:c.230_231delinsGT ENSP00000514757.1:p.Asp77Gly
ENST00000700022.1:c.275_276delinsGT ENSP00000514758.1:p.Asp92Gly
ENST00000700029.1:c.109_110delinsGT
ENST00000700029.2:c.275_276delinsGT ENSP00000514759.2:p.Asp92Gly
ENST00000706954.1:c.275_276delinsGT ENSP00000516674.1:p.Asp92Gly
ENST00000706955.1:c.*310_*311delinsGT ENSP00000516675.1:n.*310_*311delinsGT
ENST00000710265.1:c.275_276delinsGT ENSP00000518161.1:p.Asp92Gly
XM_006717926.2:c.230_231delinsGT XP_006717989.1:p.Asp77Gly
XM_011539981.1:c.275_276delinsGT XP_011538283.1:p.Asp92Gly
XM_011539982.1:c.179_180delinsGT XP_011538284.1:p.Asp60Gly
XR_945789.1:n.987_988delinsGT
XR_945790.1:n.987_988delinsGT
XR_945791.1:n.987_988delinsGT