Canonical Allele Identifier: CA1926143105

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863563G= , CM000672.2:g.87863563G= GRCh38
NC_000010.10:g.89623320G= , CM000672.1:g.89623320G= GRCh37
NC_000010.9:g.89613300G= NCBI36
NG_007466.2:g.5126G= , LRG_311:g.5126G=
NG_033079.1:g.4875C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-891G= (PTEN) ENSP00000516674.1:n.-16-891G=
ENST00000688308.1:c.-17+450G= (PTEN) ENSP00000508752.1:n.-17+450G=
ENST00000692337.1:c.5G= (MLDHR) ENSP00000509326.1:p.Trp2=
ENST00000693560.1:c.-387G= (PTEN) ENSP00000509861.1:n.-387G=
ENST00000371953.7:c.-907G= (PTEN) ENSP00000361021.3:n.-907G=
ENST00000610634.1:c.-1009G= (PTEN) ENSP00000477517.1:n.-1009G=
NM_000314.5:c.-906G= (PTEN) NP_000305.3:n.-906G=
NM_000314.6:c.-906G= (PTEN) NP_000305.3:n.-906G=
NM_001304717.2:c.-387G= (PTEN) NP_001291646.2:n.-387G=
NM_001304718.1:c.-1611G= (PTEN) NP_001291647.1:n.-1611G=