Canonical Allele Identifier: CA1926143018
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863471T= , CM000672.2:g.87863471T= GRCh38
NC_000010.10:g.89623228T= , CM000672.1:g.89623228T= GRCh37
NC_000010.9:g.89613208T= NCBI36
NG_007466.2:g.5034T= , LRG_311:g.5034T=
NG_033079.1:g.4967A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+829T= (PTEN) ENSP00000516674.1:n.-17+829T=
ENST00000688308.1:c.-17+358T= (PTEN) ENSP00000508752.1:n.-17+358T=
ENST00000693560.1:c.-479T= (PTEN) ENSP00000509861.1:n.-479T=
ENST00000445946.5:c.-984A= (KLLN) MANE Select ENSP00000392204.2:n.-984A=
ENST00000371953.7:c.-999T= (PTEN) ENSP00000361021.3:n.-999T=
ENST00000610634.1:c.-1101T= (PTEN) ENSP00000477517.1:n.-1101T=
NM_000314.5:c.-998T= (PTEN) NP_000305.3:n.-998T=
NM_000314.6:c.-998T= (PTEN) NP_000305.3:n.-998T=
NM_001304717.2:c.-479T= (PTEN) NP_001291646.2:n.-479T=
NM_001304718.1:c.-1703T= (PTEN) NP_001291647.1:n.-1703T=
NM_001126049.2:c.-984A= (KLLN) MANE Select NP_001119521.1:n.-984A=
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