Canonical Allele Identifier: CA1926143116
Gene: PTEN HGNC NCBI
MLDHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863572_87863574delinsCTT , CM000672.2:g.87863572_87863574delinsCTT GRCh38
NC_000010.10:g.89623329_89623331delinsCTT , CM000672.1:g.89623329_89623331delinsCTT GRCh37
NC_000010.9:g.89613309_89613311delinsCTT NCBI36
NG_007466.2:g.5135_5137delinsCTT , LRG_311:g.5135_5137delinsCTT
NG_033079.1:g.4864_4866delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-882_-16-880delinsCTT (PTEN) ENSP00000516674.1:n.-16-882_-16-880delinsCTT
ENST00000688308.1:c.-17+459_-17+461delinsCTT (PTEN) ENSP00000508752.1:n.-17+459_-17+461delinsCTT
ENST00000692337.1:c.14_16delinsCTT (MLDHR) ENSP00000509326.1:p.Ser5=
ENST00000693560.1:c.-378_-376delinsCTT (PTEN) ENSP00000509861.1:n.-378_-376delinsCTT
ENST00000371953.7:c.-898_-896delinsCTT (PTEN) ENSP00000361021.3:n.-898_-896delinsCTT
ENST00000610634.1:c.-1000_-998delinsCTT (PTEN) ENSP00000477517.1:n.-1000_-998delinsCTT
NM_000314.5:c.-897_-895delinsCTT (PTEN) NP_000305.3:n.-897_-895delinsCTT
NM_000314.6:c.-897_-895delinsCTT (PTEN) NP_000305.3:n.-897_-895delinsCTT
NM_001304717.2:c.-378_-376delinsCTT (PTEN) NP_001291646.2:n.-378_-376delinsCTT
NM_001304718.1:c.-1602_-1600delinsCTT (PTEN) NP_001291647.1:n.-1602_-1600delinsCTT
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