Canonical Allele Identifier: CA1926143022
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863475T= , CM000672.2:g.87863475T= GRCh38
NC_000010.10:g.89623232T= , CM000672.1:g.89623232T= GRCh37
NC_000010.9:g.89613212T= NCBI36
NG_007466.2:g.5038T= , LRG_311:g.5038T=
NG_033079.1:g.4963A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+833T= (PTEN) ENSP00000516674.1:n.-17+833T=
ENST00000688308.1:c.-17+362T= (PTEN) ENSP00000508752.1:n.-17+362T=
ENST00000693560.1:c.-475T= (PTEN) ENSP00000509861.1:n.-475T=
ENST00000445946.5:c.-988A= (KLLN) MANE Select ENSP00000392204.2:n.-988A=
ENST00000371953.7:c.-995T= (PTEN) ENSP00000361021.3:n.-995T=
ENST00000610634.1:c.-1097T= (PTEN) ENSP00000477517.1:n.-1097T=
NM_000314.5:c.-994T= (PTEN) NP_000305.3:n.-994T=
NM_000314.6:c.-994T= (PTEN) NP_000305.3:n.-994T=
NM_001304717.2:c.-475T= (PTEN) NP_001291646.2:n.-475T=
NM_001304718.1:c.-1699T= (PTEN) NP_001291647.1:n.-1699T=
NM_001126049.2:c.-988A= (KLLN) MANE Select NP_001119521.1:n.-988A=
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