Canonical Allele Identifier: CA1926142682

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863052G= , CM000672.2:g.87863052G= GRCh38
NC_000010.10:g.89622809G= , CM000672.1:g.89622809G= GRCh37
NC_000010.9:g.89612789G= NCBI36
NG_007466.2:g.4615G= , LRG_311:g.4615G=
NG_033079.1:g.5386C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+410G= (PTEN) ENSP00000516674.1:n.-17+410G=
ENST00000688308.1:c.-78G= (PTEN) ENSP00000508752.1:n.-78G=
ENST00000445946.5:c.-565C= (KLLN) MANE Select ENSP00000392204.2:n.-565C=
ENST00000445946.3:c.-565C= (KLLN) ENSP00000392204.2:n.-565C=
NM_001126049.1:c.-565C= (KLLN) NP_001119521.1:n.-565C=
NM_001126049.2:c.-565C= (KLLN) MANE Select NP_001119521.1:n.-565C=