Canonical Allele Identifier: CA2610046320

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863502del , CM000672.2:g.87863502del GRCh38
NC_000010.10:g.89623259del , CM000672.1:g.89623259del GRCh37
NC_000010.9:g.89613239del NCBI36
NG_007466.2:g.5065del , LRG_311:g.5065del
NG_033079.1:g.4936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+860del (PTEN) ENSP00000516674.1:n.-17+860del
ENST00000688308.1:c.-17+389del (PTEN) ENSP00000508752.1:n.-17+389del
ENST00000693560.1:c.-448del (PTEN) ENSP00000509861.1:n.-448del
ENST00000445946.5:c.-1015del (KLLN) MANE Select ENSP00000392204.2:n.-1015del
ENST00000371953.7:c.-968del (PTEN) ENSP00000361021.3:n.-968del
ENST00000610634.1:c.-1070del (PTEN) ENSP00000477517.1:n.-1070del
NM_000314.5:c.-967del (PTEN) NP_000305.3:n.-967del
NM_000314.6:c.-967del (PTEN) NP_000305.3:n.-967del
NM_001304717.2:c.-448del (PTEN) NP_001291646.2:n.-448del
NM_001304718.1:c.-1672del (PTEN) NP_001291647.1:n.-1672del
NM_001126049.2:c.-1015del (KLLN) MANE Select NP_001119521.1:n.-1015del