Canonical Allele Identifier: CA1926143028
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863480T= , CM000672.2:g.87863480T= GRCh38
NC_000010.10:g.89623237T= , CM000672.1:g.89623237T= GRCh37
NC_000010.9:g.89613217T= NCBI36
NG_007466.2:g.5043T= , LRG_311:g.5043T=
NG_033079.1:g.4958A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+838T= (PTEN) ENSP00000516674.1:n.-17+838T=
ENST00000688308.1:c.-17+367T= (PTEN) ENSP00000508752.1:n.-17+367T=
ENST00000693560.1:c.-470T= (PTEN) ENSP00000509861.1:n.-470T=
ENST00000445946.5:c.-993A= (KLLN) MANE Select ENSP00000392204.2:n.-993A=
ENST00000371953.7:c.-990T= (PTEN) ENSP00000361021.3:n.-990T=
ENST00000610634.1:c.-1092T= (PTEN) ENSP00000477517.1:n.-1092T=
NM_000314.5:c.-989T= (PTEN) NP_000305.3:n.-989T=
NM_000314.6:c.-989T= (PTEN) NP_000305.3:n.-989T=
NM_001304717.2:c.-470T= (PTEN) NP_001291646.2:n.-470T=
NM_001304718.1:c.-1694T= (PTEN) NP_001291647.1:n.-1694T=
NM_001126049.2:c.-993A= (KLLN) MANE Select NP_001119521.1:n.-993A=
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