Canonical Allele Identifier: CA1926143147

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863612G= , CM000672.2:g.87863612G= GRCh38
NC_000010.10:g.89623369G= , CM000672.1:g.89623369G= GRCh37
NC_000010.9:g.89613349G= NCBI36
NG_007466.2:g.5175G= , LRG_311:g.5175G=
NG_033079.1:g.4826C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-842G= (PTEN) ENSP00000516674.1:n.-16-842G=
ENST00000688308.1:c.-17+499G= (PTEN) ENSP00000508752.1:n.-17+499G=
ENST00000692337.1:c.54G= (MLDHR) ENSP00000509326.1:p.Thr18=
ENST00000693560.1:c.-338G= (PTEN) ENSP00000509861.1:n.-338G=
ENST00000371953.7:c.-858G= (PTEN) ENSP00000361021.3:n.-858G=
ENST00000610634.1:c.-960G= (PTEN) ENSP00000477517.1:n.-960G=
NM_000314.5:c.-857G= (PTEN) NP_000305.3:n.-857G=
NM_000314.6:c.-857G= (PTEN) NP_000305.3:n.-857G=
NM_001304717.2:c.-338G= (PTEN) NP_001291646.2:n.-338G=
NM_001304718.1:c.-1562G= (PTEN) NP_001291647.1:n.-1562G=