Canonical Allele Identifier: CA1926143198
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863670T= , CM000672.2:g.87863670T= GRCh38
NC_000010.10:g.89623427T= , CM000672.1:g.89623427T= GRCh37
NC_000010.9:g.89613407T= NCBI36
NG_007466.2:g.5233T= , LRG_311:g.5233T=
NG_033079.1:g.4768A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.-800T= ENSP00000514759.2:n.-800T=
ENST00000710265.1:c.-800T= ENSP00000518161.1:n.-800T=
ENST00000706954.1:c.-16-784T= ENSP00000516674.1:n.-16-784T=
ENST00000706955.1:c.-800T= ENSP00000516675.1:n.-800T=
ENST00000688158.1:c.-800T= ENSP00000509254.1:n.-800T=
ENST00000688308.1:c.-17+557T= ENSP00000508752.1:n.-17+557T=
ENST00000693560.1:c.-280T= ENSP00000509861.1:n.-280T=
ENST00000371953.8:c.-800T= MANE Select ENSP00000361021.3:n.-800T=
ENST00000371953.7:c.-800T= ENSP00000361021.3:n.-800T=
ENST00000610634.1:c.-902T= ENSP00000477517.1:n.-902T=
NM_000314.5:c.-799T= NP_000305.3:n.-799T=
NM_000314.6:c.-799T= NP_000305.3:n.-799T=
NM_001304717.2:c.-280T= NP_001291646.2:n.-280T=
NM_001304718.1:c.-1504T= NP_001291647.1:n.-1504T=
NM_000314.7:c.-799T= NP_000305.3:n.-799T=
NM_001304717.5:c.-280T= NP_001291646.4:n.-280T=
NM_001304718.2:c.-1504T= NP_001291647.1:n.-1504T=
NM_000314.8:c.-800T= MANE Select NP_000305.3:n.-800T=