Canonical Allele Identifier: CA1926143050

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863507_87863508delinsGC , CM000672.2:g.87863507_87863508delinsGC GRCh38
NC_000010.10:g.89623264_89623265delinsGC , CM000672.1:g.89623264_89623265delinsGC GRCh37
NC_000010.9:g.89613244_89613245delinsGC NCBI36
NG_007466.2:g.5070_5071delinsGC , LRG_311:g.5070_5071delinsGC
NG_033079.1:g.4930_4931delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+865_-17+866delinsGC (PTEN) ENSP00000516674.1:n.-17+865_-17+866delinsGC
ENST00000688308.1:c.-17+394_-17+395delinsGC (PTEN) ENSP00000508752.1:n.-17+394_-17+395delinsGC
ENST00000693560.1:c.-443_-442delinsGC (PTEN) ENSP00000509861.1:n.-443_-442delinsGC
ENST00000445946.5:c.-1021_-1020delinsGC (KLLN) MANE Select ENSP00000392204.2:n.-1021_-1020delinsGC
ENST00000371953.7:c.-963_-962delinsGC (PTEN) ENSP00000361021.3:n.-963_-962delinsGC
ENST00000610634.1:c.-1065_-1064delinsGC (PTEN) ENSP00000477517.1:n.-1065_-1064delinsGC
NM_000314.5:c.-962_-961delinsGC (PTEN) NP_000305.3:n.-962_-961delinsGC
NM_000314.6:c.-962_-961delinsGC (PTEN) NP_000305.3:n.-962_-961delinsGC
NM_001304717.2:c.-443_-442delinsGC (PTEN) NP_001291646.2:n.-443_-442delinsGC
NM_001304718.1:c.-1667_-1666delinsGC (PTEN) NP_001291647.1:n.-1667_-1666delinsGC
NM_001126049.2:c.-1021_-1020delinsGC (KLLN) MANE Select NP_001119521.1:n.-1021_-1020delinsGC