Canonical Allele Identifier: CA2610046338

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863510C>A , CM000672.2:g.87863510C>A GRCh38
NC_000010.10:g.89623267C>A , CM000672.1:g.89623267C>A GRCh37
NC_000010.9:g.89613247C>A NCBI36
NG_007466.2:g.5073C>A , LRG_311:g.5073C>A
NG_033079.1:g.4928G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+868C>A (PTEN) ENSP00000516674.1:n.-17+868C>A
ENST00000688308.1:c.-17+397C>A (PTEN) ENSP00000508752.1:n.-17+397C>A
ENST00000693560.1:c.-440C>A (PTEN) ENSP00000509861.1:n.-440C>A
ENST00000445946.5:c.-1023G>T (KLLN) MANE Select ENSP00000392204.2:n.-1023G>T
ENST00000371953.7:c.-960C>A (PTEN) ENSP00000361021.3:n.-960C>A
ENST00000610634.1:c.-1062C>A (PTEN) ENSP00000477517.1:n.-1062C>A
NM_000314.5:c.-959C>A (PTEN) NP_000305.3:n.-959C>A
NM_000314.6:c.-959C>A (PTEN) NP_000305.3:n.-959C>A
NM_001304717.2:c.-440C>A (PTEN) NP_001291646.2:n.-440C>A
NM_001304718.1:c.-1664C>A (PTEN) NP_001291647.1:n.-1664C>A
NM_001126049.2:c.-1023G>T (KLLN) MANE Select NP_001119521.1:n.-1023G>T