Canonical Allele Identifier: CA1926143104

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863562T= , CM000672.2:g.87863562T= GRCh38
NC_000010.10:g.89623319T= , CM000672.1:g.89623319T= GRCh37
NC_000010.9:g.89613299T= NCBI36
NG_007466.2:g.5125T= , LRG_311:g.5125T=
NG_033079.1:g.4876A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-892T= (PTEN) ENSP00000516674.1:n.-16-892T=
ENST00000688308.1:c.-17+449T= (PTEN) ENSP00000508752.1:n.-17+449T=
ENST00000692337.1:c.4T= (MLDHR) ENSP00000509326.1:p.Trp2=
ENST00000693560.1:c.-388T= (PTEN) ENSP00000509861.1:n.-388T=
ENST00000371953.7:c.-908T= (PTEN) ENSP00000361021.3:n.-908T=
ENST00000610634.1:c.-1010T= (PTEN) ENSP00000477517.1:n.-1010T=
NM_000314.5:c.-907T= (PTEN) NP_000305.3:n.-907T=
NM_000314.6:c.-907T= (PTEN) NP_000305.3:n.-907T=
NM_001304717.2:c.-388T= (PTEN) NP_001291646.2:n.-388T=
NM_001304718.1:c.-1612T= (PTEN) NP_001291647.1:n.-1612T=