Canonical Allele Identifier: CA1139768731

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863609G>T , CM000672.2:g.87863609G>T GRCh38
NC_000010.10:g.89623366G>T , CM000672.1:g.89623366G>T GRCh37
NC_000010.9:g.89613346G>T NCBI36
NG_007466.2:g.5172G>T , LRG_311:g.5172G>T
NG_033079.1:g.4829C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-845G>T (PTEN) ENSP00000516674.1:n.-16-845G>T
ENST00000688308.1:c.-17+496G>T (PTEN) ENSP00000508752.1:n.-17+496G>T
ENST00000692337.1:c.51G>T (MLDHR) ENSP00000509326.1:p.Gly17=
ENST00000693560.1:c.-341G>T (PTEN) ENSP00000509861.1:n.-341G>T
ENST00000371953.7:c.-861G>T (PTEN) ENSP00000361021.3:n.-861G>T
ENST00000610634.1:c.-963G>T (PTEN) ENSP00000477517.1:n.-963G>T
NM_000314.5:c.-860G>T (PTEN) NP_000305.3:n.-860G>T
NM_000314.6:c.-860G>T (PTEN) NP_000305.3:n.-860G>T
NM_001304717.2:c.-341G>T (PTEN) NP_001291646.2:n.-341G>T
NM_001304718.1:c.-1565G>T (PTEN) NP_001291647.1:n.-1565G>T