Canonical Allele Identifier: CA1926143166
Gene: PTEN HGNC NCBI
MLDHR HGNC NCBI

Linked Data

dbSNP Id: rs1858341362
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863631_87863632del , CM000672.2:g.87863631_87863632del GRCh38
NC_000010.10:g.89623388_89623389del , CM000672.1:g.89623388_89623389del GRCh37
NC_000010.9:g.89613368_89613369del NCBI36
NG_007466.2:g.5194_5195del , LRG_311:g.5194_5195del
NG_033079.1:g.4810_4811del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-839_-838del (PTEN) ENSP00000514759.2:n.-839_-838del
ENST00000710265.1:c.-839_-838del (PTEN) ENSP00000518161.1:n.-839_-838del
ENST00000706954.1:c.-16-823_-16-822del (PTEN) ENSP00000516674.1:n.-16-823_-16-822del
ENST00000706955.1:c.-839_-838del (PTEN) ENSP00000516675.1:n.-839_-838del
ENST00000688158.1:c.-839_-838del (PTEN) ENSP00000509254.1:n.-839_-838del
ENST00000688308.1:c.-17+518_-17+519del (PTEN) ENSP00000508752.1:n.-17+518_-17+519del
ENST00000692337.1:c.73_74del (MLDHR) ENSP00000509326.1:p.Ser25LeufsTer?
ENST00000693560.1:c.-319_-318del (PTEN) ENSP00000509861.1:n.-319_-318del
ENST00000371953.8:c.-839_-838del (PTEN) MANE Select ENSP00000361021.3:n.-839_-838del
ENST00000371953.7:c.-839_-838del (PTEN) ENSP00000361021.3:n.-839_-838del
ENST00000610634.1:c.-941_-940del (PTEN) ENSP00000477517.1:n.-941_-940del
NM_000314.5:c.-838_-837del (PTEN) NP_000305.3:n.-838_-837del
NM_000314.6:c.-838_-837del (PTEN) NP_000305.3:n.-838_-837del
NM_001304717.2:c.-319_-318del (PTEN) NP_001291646.2:n.-319_-318del
NM_001304718.1:c.-1543_-1542del (PTEN) NP_001291647.1:n.-1543_-1542del
NM_000314.7:c.-838_-837del (PTEN) NP_000305.3:n.-838_-837del
NM_001304717.5:c.-319_-318del (PTEN) NP_001291646.4:n.-319_-318del
NM_001304718.2:c.-1543_-1542del (PTEN) NP_001291647.1:n.-1543_-1542del
NM_000314.8:c.-839_-838del (PTEN) MANE Select NP_000305.3:n.-839_-838del
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