Canonical Allele Identifier: CA1926143032
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

dbSNP Id: rs1858330994
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863484dup , CM000672.2:g.87863484dup GRCh38
NC_000010.10:g.89623241dup , CM000672.1:g.89623241dup GRCh37
NC_000010.9:g.89613221dup NCBI36
NG_007466.2:g.5047dup , LRG_311:g.5047dup
NG_033079.1:g.4954dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+842dup (PTEN) ENSP00000516674.1:n.-17+842dup
ENST00000688308.1:c.-17+371dup (PTEN) ENSP00000508752.1:n.-17+371dup
ENST00000693560.1:c.-466dup (PTEN) ENSP00000509861.1:n.-466dup
ENST00000445946.5:c.-997dup (KLLN) MANE Select ENSP00000392204.2:n.-997dup
ENST00000371953.7:c.-986dup (PTEN) ENSP00000361021.3:n.-986dup
ENST00000610634.1:c.-1088dup (PTEN) ENSP00000477517.1:n.-1088dup
NM_000314.5:c.-985dup (PTEN) NP_000305.3:n.-985dup
NM_000314.6:c.-985dup (PTEN) NP_000305.3:n.-985dup
NM_001304717.2:c.-466dup (PTEN) NP_001291646.2:n.-466dup
NM_001304718.1:c.-1690dup (PTEN) NP_001291647.1:n.-1690dup
NM_001126049.2:c.-997dup (KLLN) MANE Select NP_001119521.1:n.-997dup
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