Canonical Allele Identifier: CA1926142827
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863264G= , CM000672.2:g.87863264G= GRCh38
NC_000010.10:g.89623021G= , CM000672.1:g.89623021G= GRCh37
NC_000010.9:g.89613001G= NCBI36
NG_007466.2:g.4827G= , LRG_311:g.4827G=
NG_033079.1:g.5174C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+622G= (PTEN) ENSP00000516674.1:n.-17+622G=
ENST00000688308.1:c.-17+151G= (PTEN) ENSP00000508752.1:n.-17+151G=
ENST00000445946.5:c.-777C= (KLLN) MANE Select ENSP00000392204.2:n.-777C=
ENST00000371953.7:c.-1206G= (PTEN) ENSP00000361021.3:n.-1206G=
ENST00000445946.3:c.-777C= (KLLN) ENSP00000392204.2:n.-777C=
NM_001126049.1:c.-777C= (KLLN) NP_001119521.1:n.-777C=
NM_001126049.2:c.-777C= (KLLN) MANE Select NP_001119521.1:n.-777C=
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