Canonical Allele Identifier: CA000662
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

ClinVar Variation Id: 127686
ClinVar RCV Id: RCV000115581
dbSNP Id: rs587780002
MyVariant Identifiers: chr10:g.89623233C>G (hg19) chr10:g.87863476C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863476C>G , CM000672.2:g.87863476C>G GRCh38
NC_000010.10:g.89623233C>G , CM000672.1:g.89623233C>G GRCh37
NC_000010.9:g.89613213C>G NCBI36
NG_007466.2:g.5039C>G , LRG_311:g.5039C>G
NG_033079.1:g.4962G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+834C>G (PTEN) ENSP00000516674.1:n.-17+834C>G
ENST00000688308.1:c.-17+363C>G (PTEN) ENSP00000508752.1:n.-17+363C>G
ENST00000693560.1:c.-474C>G (PTEN) ENSP00000509861.1:n.-474C>G
ENST00000445946.5:c.-989G>C (KLLN) MANE Select ENSP00000392204.2:n.-989G>C
ENST00000371953.7:c.-994C>G (PTEN) ENSP00000361021.3:n.-994C>G
ENST00000610634.1:c.-1096C>G (PTEN) ENSP00000477517.1:n.-1096C>G
NM_000314.5:c.-993C>G (PTEN) NP_000305.3:n.-993C>G
NM_000314.6:c.-993C>G (PTEN) NP_000305.3:n.-993C>G
NM_001304717.2:c.-474C>G (PTEN) NP_001291646.2:n.-474C>G
NM_001304718.1:c.-1698C>G (PTEN) NP_001291647.1:n.-1698C>G
NM_001126049.2:c.-989G>C (KLLN) MANE Select NP_001119521.1:n.-989G>C
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