Canonical Allele Identifier: CA1926143039
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863495G= , CM000672.2:g.87863495G= GRCh38
NC_000010.10:g.89623252G= , CM000672.1:g.89623252G= GRCh37
NC_000010.9:g.89613232G= NCBI36
NG_007466.2:g.5058G= , LRG_311:g.5058G=
NG_033079.1:g.4943C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+853G= (PTEN) ENSP00000516674.1:n.-17+853G=
ENST00000688308.1:c.-17+382G= (PTEN) ENSP00000508752.1:n.-17+382G=
ENST00000693560.1:c.-455G= (PTEN) ENSP00000509861.1:n.-455G=
ENST00000445946.5:c.-1008C= (KLLN) MANE Select ENSP00000392204.2:n.-1008C=
ENST00000371953.7:c.-975G= (PTEN) ENSP00000361021.3:n.-975G=
ENST00000610634.1:c.-1077G= (PTEN) ENSP00000477517.1:n.-1077G=
NM_000314.5:c.-974G= (PTEN) NP_000305.3:n.-974G=
NM_000314.6:c.-974G= (PTEN) NP_000305.3:n.-974G=
NM_001304717.2:c.-455G= (PTEN) NP_001291646.2:n.-455G=
NM_001304718.1:c.-1679G= (PTEN) NP_001291647.1:n.-1679G=
NM_001126049.2:c.-1008C= (KLLN) MANE Select NP_001119521.1:n.-1008C=
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