Canonical Allele Identifier: CA1926143125
Gene: PTEN HGNC NCBI
MLDHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863582T= , CM000672.2:g.87863582T= GRCh38
NC_000010.10:g.89623339T= , CM000672.1:g.89623339T= GRCh37
NC_000010.9:g.89613319T= NCBI36
NG_007466.2:g.5145T= , LRG_311:g.5145T=
NG_033079.1:g.4856A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-872T= (PTEN) ENSP00000516674.1:n.-16-872T=
ENST00000688308.1:c.-17+469T= (PTEN) ENSP00000508752.1:n.-17+469T=
ENST00000692337.1:c.24T= (MLDHR) ENSP00000509326.1:p.Ala8=
ENST00000693560.1:c.-368T= (PTEN) ENSP00000509861.1:n.-368T=
ENST00000371953.7:c.-888T= (PTEN) ENSP00000361021.3:n.-888T=
ENST00000610634.1:c.-990T= (PTEN) ENSP00000477517.1:n.-990T=
NM_000314.5:c.-887T= (PTEN) NP_000305.3:n.-887T=
NM_000314.6:c.-887T= (PTEN) NP_000305.3:n.-887T=
NM_001304717.2:c.-368T= (PTEN) NP_001291646.2:n.-368T=
NM_001304718.1:c.-1592T= (PTEN) NP_001291647.1:n.-1592T=
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