Canonical Allele Identifier: CA1926143139

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863605C= , CM000672.2:g.87863605C= GRCh38
NC_000010.10:g.89623362C= , CM000672.1:g.89623362C= GRCh37
NC_000010.9:g.89613342C= NCBI36
NG_007466.2:g.5168C= , LRG_311:g.5168C=
NG_033079.1:g.4833G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-849C= (PTEN) ENSP00000516674.1:n.-16-849C=
ENST00000688308.1:c.-17+492C= (PTEN) ENSP00000508752.1:n.-17+492C=
ENST00000692337.1:c.47C= (MLDHR) ENSP00000509326.1:p.Ala16=
ENST00000693560.1:c.-345C= (PTEN) ENSP00000509861.1:n.-345C=
ENST00000371953.7:c.-865C= (PTEN) ENSP00000361021.3:n.-865C=
ENST00000610634.1:c.-967C= (PTEN) ENSP00000477517.1:n.-967C=
NM_000314.5:c.-864C= (PTEN) NP_000305.3:n.-864C=
NM_000314.6:c.-864C= (PTEN) NP_000305.3:n.-864C=
NM_001304717.2:c.-345C= (PTEN) NP_001291646.2:n.-345C=
NM_001304718.1:c.-1569C= (PTEN) NP_001291647.1:n.-1569C=