Canonical Allele Identifier: CA1926177108
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967659T= , CM000672.2:g.87967659T= GRCh38
NC_000010.10:g.89727416T= , CM000672.1:g.89727416T= GRCh37
NC_000010.9:g.89717396T= NCBI36
NG_007466.2:g.109221T= , LRG_311:g.109221T=

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*2428T= ENSP00000518161.1:n.*2428T=
ENST00000688158.2:n.4134T=
ENST00000706954.1:c.*2187T= ENSP00000516674.1:n.*2187T=
ENST00000706955.1:c.*3434T= ENSP00000516675.1:n.*3434T=
ENST00000688158.1:c.*3510T= ENSP00000509254.1:n.*3510T=
ENST00000693560.1:c.*2187T= ENSP00000509861.1:n.*2187T=
ENST00000371953.8:c.*2187T= MANE Select ENSP00000361021.3:n.*2187T=
ENST00000371953.7:c.*2187T= ENSP00000361021.3:n.*2187T=
NM_000314.5:c.*2187T= NP_000305.3:n.*2187T=
NM_000314.6:c.*2187T= NP_000305.3:n.*2187T=
NM_001304717.2:c.*2187T= NP_001291646.2:n.*2187T=
NM_001304718.1:c.*2187T= NP_001291647.1:n.*2187T=
XM_006717926.2:c.*2187T= XP_006717989.1:n.*2187T=
XM_011539982.1:c.*2187T= XP_011538284.1:n.*2187T=
XR_945791.1:n.3969T=
NM_000314.7:c.*2187T= NP_000305.3:n.*2187T=
NM_001304717.5:c.*2187T= NP_001291646.4:n.*2187T=
NM_001304718.2:c.*2187T= NP_001291647.1:n.*2187T=
NM_000314.8:c.*2187T= MANE Select NP_000305.3:n.*2187T=