Canonical Allele Identifier: CA1926143155

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863619C= , CM000672.2:g.87863619C= GRCh38
NC_000010.10:g.89623376C= , CM000672.1:g.89623376C= GRCh37
NC_000010.9:g.89613356C= NCBI36
NG_007466.2:g.5182C= , LRG_311:g.5182C=
NG_033079.1:g.4819G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-835C= (PTEN) ENSP00000516674.1:n.-16-835C=
ENST00000688308.1:c.-17+506C= (PTEN) ENSP00000508752.1:n.-17+506C=
ENST00000692337.1:c.61C= (MLDHR) ENSP00000509326.1:p.Arg21=
ENST00000693560.1:c.-331C= (PTEN) ENSP00000509861.1:n.-331C=
ENST00000371953.7:c.-851C= (PTEN) ENSP00000361021.3:n.-851C=
ENST00000610634.1:c.-953C= (PTEN) ENSP00000477517.1:n.-953C=
NM_000314.5:c.-850C= (PTEN) NP_000305.3:n.-850C=
NM_000314.6:c.-850C= (PTEN) NP_000305.3:n.-850C=
NM_001304717.2:c.-331C= (PTEN) NP_001291646.2:n.-331C=
NM_001304718.1:c.-1555C= (PTEN) NP_001291647.1:n.-1555C=