Canonical Allele Identifier: CA338721
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 220416

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960843_87960880del , CM000672.2:g.87960843_87960880del GRCh38
NC_000010.10:g.89720600_89720637del , CM000672.1:g.89720600_89720637del GRCh37
NC_000010.9:g.89710580_89710617del NCBI36
NG_007466.2:g.102405_102442del , LRG_311:g.102405_102442del

Transcript Alleles

HGVS Amino-acid change
ENST00000371953.8:c.802-51_802-14del MANE Select ENSP00000361021.3:p.=
ENST00000371953.7:c.802-51_802-14del ENSP00000361021.3:p.=
ENST00000472832.2:n.229-51_229-14del ENSP00000483066.1:p.=
NM_000314.5:c.802-51_802-14del NP_000305.3:p.=
NM_000314.6:c.802-51_802-14del NP_000305.3:p.=
NM_001304717.2:c.1321-51_1321-14del NP_001291646.2:p.=
NM_001304718.1:c.211-51_211-14del NP_001291647.1:p.=
XM_006717926.2:c.757-51_757-14del XP_006717989.1:p.=
XM_011539981.1:c.802-51_802-14del XP_011538283.1:p.=
XM_011539982.1:c.706-51_706-14del XP_011538284.1:p.=
XR_945791.1:n.1372-51_1372-14del
NM_000314.7:c.802-51_802-14del NP_000305.3:p.=
NM_001304717.5:c.1321-51_1321-14del NP_001291646.4:p.=
NM_001304718.2:c.211-51_211-14del NP_001291647.1:p.=
NM_000314.8:c.802-51_802-14del MANE Select NP_000305.3:p.=