Canonical Allele Identifier: CA1926143153

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863617T= , CM000672.2:g.87863617T= GRCh38
NC_000010.10:g.89623374T= , CM000672.1:g.89623374T= GRCh37
NC_000010.9:g.89613354T= NCBI36
NG_007466.2:g.5180T= , LRG_311:g.5180T=
NG_033079.1:g.4821A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-837T= (PTEN) ENSP00000516674.1:n.-16-837T=
ENST00000688308.1:c.-17+504T= (PTEN) ENSP00000508752.1:n.-17+504T=
ENST00000692337.1:c.59T= (MLDHR) ENSP00000509326.1:p.Leu20=
ENST00000693560.1:c.-333T= (PTEN) ENSP00000509861.1:n.-333T=
ENST00000371953.7:c.-853T= (PTEN) ENSP00000361021.3:n.-853T=
ENST00000610634.1:c.-955T= (PTEN) ENSP00000477517.1:n.-955T=
NM_000314.5:c.-852T= (PTEN) NP_000305.3:n.-852T=
NM_000314.6:c.-852T= (PTEN) NP_000305.3:n.-852T=
NM_001304717.2:c.-333T= (PTEN) NP_001291646.2:n.-333T=
NM_001304718.1:c.-1557T= (PTEN) NP_001291647.1:n.-1557T=