Canonical Allele Identifier: CA1926143020
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863473G= , CM000672.2:g.87863473G= GRCh38
NC_000010.10:g.89623230G= , CM000672.1:g.89623230G= GRCh37
NC_000010.9:g.89613210G= NCBI36
NG_007466.2:g.5036G= , LRG_311:g.5036G=
NG_033079.1:g.4965C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+831G= (PTEN) ENSP00000516674.1:n.-17+831G=
ENST00000688308.1:c.-17+360G= (PTEN) ENSP00000508752.1:n.-17+360G=
ENST00000693560.1:c.-477G= (PTEN) ENSP00000509861.1:n.-477G=
ENST00000445946.5:c.-986C= (KLLN) MANE Select ENSP00000392204.2:n.-986C=
ENST00000371953.7:c.-997G= (PTEN) ENSP00000361021.3:n.-997G=
ENST00000610634.1:c.-1099G= (PTEN) ENSP00000477517.1:n.-1099G=
NM_000314.5:c.-996G= (PTEN) NP_000305.3:n.-996G=
NM_000314.6:c.-996G= (PTEN) NP_000305.3:n.-996G=
NM_001304717.2:c.-477G= (PTEN) NP_001291646.2:n.-477G=
NM_001304718.1:c.-1701G= (PTEN) NP_001291647.1:n.-1701G=
NM_001126049.2:c.-986C= (KLLN) MANE Select NP_001119521.1:n.-986C=
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