Canonical Allele Identifier: CA1926143019

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863472C= , CM000672.2:g.87863472C= GRCh38
NC_000010.10:g.89623229C= , CM000672.1:g.89623229C= GRCh37
NC_000010.9:g.89613209C= NCBI36
NG_007466.2:g.5035C= , LRG_311:g.5035C=
NG_033079.1:g.4966G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+830C= (PTEN) ENSP00000516674.1:n.-17+830C=
ENST00000688308.1:c.-17+359C= (PTEN) ENSP00000508752.1:n.-17+359C=
ENST00000693560.1:c.-478C= (PTEN) ENSP00000509861.1:n.-478C=
ENST00000445946.5:c.-985G= (KLLN) MANE Select ENSP00000392204.2:n.-985G=
ENST00000371953.7:c.-998C= (PTEN) ENSP00000361021.3:n.-998C=
ENST00000610634.1:c.-1100C= (PTEN) ENSP00000477517.1:n.-1100C=
NM_000314.5:c.-997C= (PTEN) NP_000305.3:n.-997C=
NM_000314.6:c.-997C= (PTEN) NP_000305.3:n.-997C=
NM_001304717.2:c.-478C= (PTEN) NP_001291646.2:n.-478C=
NM_001304718.1:c.-1702C= (PTEN) NP_001291647.1:n.-1702C=
NM_001126049.2:c.-985G= (KLLN) MANE Select NP_001119521.1:n.-985G=