Canonical Allele Identifier: CA1926142912

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863349T= , CM000672.2:g.87863349T= GRCh38
NC_000010.10:g.89623106T= , CM000672.1:g.89623106T= GRCh37
NC_000010.9:g.89613086T= NCBI36
NG_007466.2:g.4912T= , LRG_311:g.4912T=
NG_033079.1:g.5089A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+707T= (PTEN) ENSP00000516674.1:n.-17+707T=
ENST00000688308.1:c.-17+236T= (PTEN) ENSP00000508752.1:n.-17+236T=
ENST00000445946.5:c.-862A= (KLLN) MANE Select ENSP00000392204.2:n.-862A=
ENST00000371953.7:c.-1121T= (PTEN) ENSP00000361021.3:n.-1121T=
ENST00000445946.3:c.-862A= (KLLN) ENSP00000392204.2:n.-862A=
NM_001126049.1:c.-862A= (KLLN) NP_001119521.1:n.-862A=
NM_001126049.2:c.-862A= (KLLN) MANE Select NP_001119521.1:n.-862A=