Canonical Allele Identifier: CA2788894869

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863532A>T , CM000672.2:g.87863532A>T GRCh38
NC_000010.10:g.89623289A>T , CM000672.1:g.89623289A>T GRCh37
NC_000010.9:g.89613269A>T NCBI36
NG_007466.2:g.5095A>T , LRG_311:g.5095A>T
NG_033079.1:g.4906T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+890A>T (PTEN) ENSP00000516674.1:n.-17+890A>T
ENST00000688308.1:c.-17+419A>T (PTEN) ENSP00000508752.1:n.-17+419A>T
ENST00000693560.1:c.-418A>T (PTEN) ENSP00000509861.1:n.-418A>T
ENST00000445946.5:c.-1045T>A (KLLN) MANE Select ENSP00000392204.2:n.-1045T>A
ENST00000371953.7:c.-938A>T (PTEN) ENSP00000361021.3:n.-938A>T
ENST00000610634.1:c.-1040A>T (PTEN) ENSP00000477517.1:n.-1040A>T
NM_000314.5:c.-937A>T (PTEN) NP_000305.3:n.-937A>T
NM_000314.6:c.-937A>T (PTEN) NP_000305.3:n.-937A>T
NM_001304717.2:c.-418A>T (PTEN) NP_001291646.2:n.-418A>T
NM_001304718.1:c.-1642A>T (PTEN) NP_001291647.1:n.-1642A>T
NM_001126049.2:c.-1045T>A (KLLN) MANE Select NP_001119521.1:n.-1045T>A