Canonical Allele Identifier: CA1926143165
Gene: PTEN HGNC NCBI
MLDHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863626T= , CM000672.2:g.87863626T= GRCh38
NC_000010.10:g.89623383T= , CM000672.1:g.89623383T= GRCh37
NC_000010.9:g.89613363T= NCBI36
NG_007466.2:g.5189T= , LRG_311:g.5189T=
NG_033079.1:g.4812A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-844T= (PTEN) ENSP00000514759.2:n.-844T=
ENST00000710265.1:c.-844T= (PTEN) ENSP00000518161.1:n.-844T=
ENST00000706954.1:c.-16-828T= (PTEN) ENSP00000516674.1:n.-16-828T=
ENST00000706955.1:c.-844T= (PTEN) ENSP00000516675.1:n.-844T=
ENST00000688158.1:c.-844T= (PTEN) ENSP00000509254.1:n.-844T=
ENST00000688308.1:c.-17+513T= (PTEN) ENSP00000508752.1:n.-17+513T=
ENST00000692337.1:c.68T= (MLDHR) ENSP00000509326.1:p.Val23=
ENST00000693560.1:c.-324T= (PTEN) ENSP00000509861.1:n.-324T=
ENST00000371953.8:c.-844T= (PTEN) MANE Select ENSP00000361021.3:n.-844T=
ENST00000371953.7:c.-844T= (PTEN) ENSP00000361021.3:n.-844T=
ENST00000610634.1:c.-946T= (PTEN) ENSP00000477517.1:n.-946T=
NM_000314.5:c.-843T= (PTEN) NP_000305.3:n.-843T=
NM_000314.6:c.-843T= (PTEN) NP_000305.3:n.-843T=
NM_001304717.2:c.-324T= (PTEN) NP_001291646.2:n.-324T=
NM_001304718.1:c.-1548T= (PTEN) NP_001291647.1:n.-1548T=
NM_000314.7:c.-843T= (PTEN) NP_000305.3:n.-843T=
NM_001304717.5:c.-324T= (PTEN) NP_001291646.4:n.-324T=
NM_001304718.2:c.-1548T= (PTEN) NP_001291647.1:n.-1548T=
NM_000314.8:c.-844T= (PTEN) MANE Select NP_000305.3:n.-844T=
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