Canonical Allele Identifier: CA1926143127

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863594_87863601delinsCGCGCTCG , CM000672.2:g.87863594_87863601delinsCGCGCTCG GRCh38
NC_000010.10:g.89623351_89623358delinsCGCGCTCG , CM000672.1:g.89623351_89623358delinsCGCGCTCG GRCh37
NC_000010.9:g.89613331_89613338delinsCGCGCTCG NCBI36
NG_007466.2:g.5157_5164delinsCGCGCTCG , LRG_311:g.5157_5164delinsCGCGCTCG
NG_033079.1:g.4837_4844delinsCGAGCGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-860_-16-853delinsCGCGCTCG (PTEN) ENSP00000516674.1:n.-16-860_-16-853delinsCGCGCTCG
ENST00000688308.1:c.-17+481_-17+488delinsCGCGCTCG (PTEN) ENSP00000508752.1:n.-17+481_-17+488delinsCGCGCTCG
ENST00000692337.1:c.36_43delinsCGCGCTCG (MLDHR) ENSP00000509326.1:p.Tyr12=
ENST00000693560.1:c.-356_-349delinsCGCGCTCG (PTEN) ENSP00000509861.1:n.-356_-349delinsCGCGCTCG
ENST00000371953.7:c.-876_-869delinsCGCGCTCG (PTEN) ENSP00000361021.3:n.-876_-869delinsCGCGCTCG
ENST00000610634.1:c.-978_-971delinsCGCGCTCG (PTEN) ENSP00000477517.1:n.-978_-971delinsCGCGCTCG
NM_000314.5:c.-875_-868delinsCGCGCTCG (PTEN) NP_000305.3:n.-875_-868delinsCGCGCTCG
NM_000314.6:c.-875_-868delinsCGCGCTCG (PTEN) NP_000305.3:n.-875_-868delinsCGCGCTCG
NM_001304717.2:c.-356_-349delinsCGCGCTCG (PTEN) NP_001291646.2:n.-356_-349delinsCGCGCTCG
NM_001304718.1:c.-1580_-1573delinsCGCGCTCG (PTEN) NP_001291647.1:n.-1580_-1573delinsCGCGCTCG