Canonical Allele Identifier: CA1926143051

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863507G= , CM000672.2:g.87863507G= GRCh38
NC_000010.10:g.89623264G= , CM000672.1:g.89623264G= GRCh37
NC_000010.9:g.89613244G= NCBI36
NG_007466.2:g.5070G= , LRG_311:g.5070G=
NG_033079.1:g.4931C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+865G= (PTEN) ENSP00000516674.1:n.-17+865G=
ENST00000688308.1:c.-17+394G= (PTEN) ENSP00000508752.1:n.-17+394G=
ENST00000693560.1:c.-443G= (PTEN) ENSP00000509861.1:n.-443G=
ENST00000445946.5:c.-1020C= (KLLN) MANE Select ENSP00000392204.2:n.-1020C=
ENST00000371953.7:c.-963G= (PTEN) ENSP00000361021.3:n.-963G=
ENST00000610634.1:c.-1065G= (PTEN) ENSP00000477517.1:n.-1065G=
NM_000314.5:c.-962G= (PTEN) NP_000305.3:n.-962G=
NM_000314.6:c.-962G= (PTEN) NP_000305.3:n.-962G=
NM_001304717.2:c.-443G= (PTEN) NP_001291646.2:n.-443G=
NM_001304718.1:c.-1667G= (PTEN) NP_001291647.1:n.-1667G=
NM_001126049.2:c.-1020C= (KLLN) MANE Select NP_001119521.1:n.-1020C=