Canonical Allele Identifier: CA1926177006
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967592T= , CM000672.2:g.87967592T= GRCh38
NC_000010.10:g.89727349T= , CM000672.1:g.89727349T= GRCh37
NC_000010.9:g.89717329T= NCBI36
NG_007466.2:g.109154T= , LRG_311:g.109154T=

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*2361T= ENSP00000518161.1:n.*2361T=
ENST00000688158.2:n.4067T=
ENST00000706954.1:c.*2120T= ENSP00000516674.1:n.*2120T=
ENST00000706955.1:c.*3367T= ENSP00000516675.1:n.*3367T=
ENST00000688158.1:c.*3443T= ENSP00000509254.1:n.*3443T=
ENST00000693560.1:c.*2120T= ENSP00000509861.1:n.*2120T=
ENST00000371953.8:c.*2120T= MANE Select ENSP00000361021.3:n.*2120T=
ENST00000371953.7:c.*2120T= ENSP00000361021.3:n.*2120T=
NM_000314.5:c.*2120T= NP_000305.3:n.*2120T=
NM_000314.6:c.*2120T= NP_000305.3:n.*2120T=
NM_001304717.2:c.*2120T= NP_001291646.2:n.*2120T=
NM_001304718.1:c.*2120T= NP_001291647.1:n.*2120T=
XM_006717926.2:c.*2120T= XP_006717989.1:n.*2120T=
XM_011539982.1:c.*2120T= XP_011538284.1:n.*2120T=
XR_945791.1:n.3902T=
NM_000314.7:c.*2120T= NP_000305.3:n.*2120T=
NM_001304717.5:c.*2120T= NP_001291646.4:n.*2120T=
NM_001304718.2:c.*2120T= NP_001291647.1:n.*2120T=
NM_000314.8:c.*2120T= MANE Select NP_000305.3:n.*2120T=