Canonical Allele Identifier: CA1926142684

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863057T= , CM000672.2:g.87863057T= GRCh38
NC_000010.10:g.89622814T= , CM000672.1:g.89622814T= GRCh37
NC_000010.9:g.89612794T= NCBI36
NG_007466.2:g.4620T= , LRG_311:g.4620T=
NG_033079.1:g.5381A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+415T= (PTEN) ENSP00000516674.1:n.-17+415T=
ENST00000688308.1:c.-73T= (PTEN) ENSP00000508752.1:n.-73T=
ENST00000445946.5:c.-570A= (KLLN) MANE Select ENSP00000392204.2:n.-570A=
ENST00000445946.3:c.-570A= (KLLN) ENSP00000392204.2:n.-570A=
NM_001126049.1:c.-570A= (KLLN) NP_001119521.1:n.-570A=
NM_001126049.2:c.-570A= (KLLN) MANE Select NP_001119521.1:n.-570A=