Canonical Allele Identifier: CA1926143073

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863532A= , CM000672.2:g.87863532A= GRCh38
NC_000010.10:g.89623289A= , CM000672.1:g.89623289A= GRCh37
NC_000010.9:g.89613269A= NCBI36
NG_007466.2:g.5095A= , LRG_311:g.5095A=
NG_033079.1:g.4906T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+890A= (PTEN) ENSP00000516674.1:n.-17+890A=
ENST00000688308.1:c.-17+419A= (PTEN) ENSP00000508752.1:n.-17+419A=
ENST00000693560.1:c.-418A= (PTEN) ENSP00000509861.1:n.-418A=
ENST00000445946.5:c.-1045T= (KLLN) MANE Select ENSP00000392204.2:n.-1045T=
ENST00000371953.7:c.-938A= (PTEN) ENSP00000361021.3:n.-938A=
ENST00000610634.1:c.-1040A= (PTEN) ENSP00000477517.1:n.-1040A=
NM_000314.5:c.-937A= (PTEN) NP_000305.3:n.-937A=
NM_000314.6:c.-937A= (PTEN) NP_000305.3:n.-937A=
NM_001304717.2:c.-418A= (PTEN) NP_001291646.2:n.-418A=
NM_001304718.1:c.-1642A= (PTEN) NP_001291647.1:n.-1642A=
NM_001126049.2:c.-1045T= (KLLN) MANE Select NP_001119521.1:n.-1045T=