Canonical Allele Identifier: CA1926143171

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863633C= , CM000672.2:g.87863633C= GRCh38
NC_000010.10:g.89623390C= , CM000672.1:g.89623390C= GRCh37
NC_000010.9:g.89613370C= NCBI36
NG_007466.2:g.5196C= , LRG_311:g.5196C=
NG_033079.1:g.4805G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-837C= (PTEN) ENSP00000514759.2:n.-837C=
ENST00000710265.1:c.-837C= (PTEN) ENSP00000518161.1:n.-837C=
ENST00000706954.1:c.-16-821C= (PTEN) ENSP00000516674.1:n.-16-821C=
ENST00000706955.1:c.-837C= (PTEN) ENSP00000516675.1:n.-837C=
ENST00000688158.1:c.-837C= (PTEN) ENSP00000509254.1:n.-837C=
ENST00000688308.1:c.-17+520C= (PTEN) ENSP00000508752.1:n.-17+520C=
ENST00000692337.1:c.75C= (MLDHR) ENSP00000509326.1:p.Ser25=
ENST00000693560.1:c.-317C= (PTEN) ENSP00000509861.1:n.-317C=
ENST00000371953.8:c.-837C= (PTEN) MANE Select ENSP00000361021.3:n.-837C=
ENST00000371953.7:c.-837C= (PTEN) ENSP00000361021.3:n.-837C=
ENST00000610634.1:c.-939C= (PTEN) ENSP00000477517.1:n.-939C=
NM_000314.5:c.-836C= (PTEN) NP_000305.3:n.-836C=
NM_000314.6:c.-836C= (PTEN) NP_000305.3:n.-836C=
NM_001304717.2:c.-317C= (PTEN) NP_001291646.2:n.-317C=
NM_001304718.1:c.-1541C= (PTEN) NP_001291647.1:n.-1541C=
NM_000314.7:c.-836C= (PTEN) NP_000305.3:n.-836C=
NM_001304717.5:c.-317C= (PTEN) NP_001291646.4:n.-317C=
NM_001304718.2:c.-1541C= (PTEN) NP_001291647.1:n.-1541C=
NM_000314.8:c.-837C= (PTEN) MANE Select NP_000305.3:n.-837C=