Canonical Allele Identifier: CA1926143123

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863579C= , CM000672.2:g.87863579C= GRCh38
NC_000010.10:g.89623336C= , CM000672.1:g.89623336C= GRCh37
NC_000010.9:g.89613316C= NCBI36
NG_007466.2:g.5142C= , LRG_311:g.5142C=
NG_033079.1:g.4859G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-875C= (PTEN) ENSP00000516674.1:n.-16-875C=
ENST00000688308.1:c.-17+466C= (PTEN) ENSP00000508752.1:n.-17+466C=
ENST00000692337.1:c.21C= (MLDHR) ENSP00000509326.1:p.Cys7=
ENST00000693560.1:c.-371C= (PTEN) ENSP00000509861.1:n.-371C=
ENST00000371953.7:c.-891C= (PTEN) ENSP00000361021.3:n.-891C=
ENST00000610634.1:c.-993C= (PTEN) ENSP00000477517.1:n.-993C=
NM_000314.5:c.-890C= (PTEN) NP_000305.3:n.-890C=
NM_000314.6:c.-890C= (PTEN) NP_000305.3:n.-890C=
NM_001304717.2:c.-371C= (PTEN) NP_001291646.2:n.-371C=
NM_001304718.1:c.-1595C= (PTEN) NP_001291647.1:n.-1595C=