Canonical Allele Identifier: CA1926142821
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863257G= , CM000672.2:g.87863257G= GRCh38
NC_000010.10:g.89623014G= , CM000672.1:g.89623014G= GRCh37
NC_000010.9:g.89612994G= NCBI36
NG_007466.2:g.4820G= , LRG_311:g.4820G=
NG_033079.1:g.5181C=

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+615G= (PTEN) ENSP00000516674.1:n.-17+615G=
ENST00000688308.1:c.-17+144G= (PTEN) ENSP00000508752.1:n.-17+144G=
ENST00000445946.5:c.-770C= (KLLN) MANE Select ENSP00000392204.2:n.-770C=
ENST00000371953.7:c.-1213G= (PTEN) ENSP00000361021.3:n.-1213G=
ENST00000445946.3:c.-770C= (KLLN) ENSP00000392204.2:n.-770C=
NM_001126049.1:c.-770C= (KLLN) NP_001119521.1:n.-770C=
NM_001126049.2:c.-770C= (KLLN) MANE Select NP_001119521.1:n.-770C=
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