Canonical Allele Identifier: CA930912746

Linked Data

dbSNP Id: rs1858337802

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863569del , CM000672.2:g.87863569del GRCh38
NC_000010.10:g.89623326del , CM000672.1:g.89623326del GRCh37
NC_000010.9:g.89613306del NCBI36
NG_007466.2:g.5132del , LRG_311:g.5132del
NG_033079.1:g.4869del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-16-885del (PTEN) ENSP00000516674.1:n.-16-885del
ENST00000688308.1:c.-17+456del (PTEN) ENSP00000508752.1:n.-17+456del
ENST00000692337.1:c.11del (MLDHR) ENSP00000509326.1:p.Asp4AlafsTer?
ENST00000693560.1:c.-381del (PTEN) ENSP00000509861.1:n.-381del
ENST00000371953.7:c.-901del (PTEN) ENSP00000361021.3:n.-901del
ENST00000610634.1:c.-1003del (PTEN) ENSP00000477517.1:n.-1003del
NM_000314.5:c.-900del (PTEN) NP_000305.3:n.-900del
NM_000314.6:c.-900del (PTEN) NP_000305.3:n.-900del
NM_001304717.2:c.-381del (PTEN) NP_001291646.2:n.-381del
NM_001304718.1:c.-1605del (PTEN) NP_001291647.1:n.-1605del