Canonical Allele Identifier: CA1926143107

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863564G= , CM000672.2:g.87863564G= GRCh38
NC_000010.10:g.89623321G= , CM000672.1:g.89623321G= GRCh37
NC_000010.9:g.89613301G= NCBI36
NG_007466.2:g.5127G= , LRG_311:g.5127G=
NG_033079.1:g.4874C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-890G= (PTEN) ENSP00000516674.1:n.-16-890G=
ENST00000688308.1:c.-17+451G= (PTEN) ENSP00000508752.1:n.-17+451G=
ENST00000692337.1:c.6G= (MLDHR) ENSP00000509326.1:p.Trp2=
ENST00000693560.1:c.-386G= (PTEN) ENSP00000509861.1:n.-386G=
ENST00000371953.7:c.-906G= (PTEN) ENSP00000361021.3:n.-906G=
ENST00000610634.1:c.-1008G= (PTEN) ENSP00000477517.1:n.-1008G=
NM_000314.5:c.-905G= (PTEN) NP_000305.3:n.-905G=
NM_000314.6:c.-905G= (PTEN) NP_000305.3:n.-905G=
NM_001304717.2:c.-386G= (PTEN) NP_001291646.2:n.-386G=
NM_001304718.1:c.-1610G= (PTEN) NP_001291647.1:n.-1610G=