Canonical Allele Identifier: CA1926142829
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863267G= , CM000672.2:g.87863267G= GRCh38
NC_000010.10:g.89623024G= , CM000672.1:g.89623024G= GRCh37
NC_000010.9:g.89613004G= NCBI36
NG_007466.2:g.4830G= , LRG_311:g.4830G=
NG_033079.1:g.5171C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+625G= (PTEN) ENSP00000516674.1:n.-17+625G=
ENST00000688308.1:c.-17+154G= (PTEN) ENSP00000508752.1:n.-17+154G=
ENST00000445946.5:c.-780C= (KLLN) MANE Select ENSP00000392204.2:n.-780C=
ENST00000371953.7:c.-1203G= (PTEN) ENSP00000361021.3:n.-1203G=
ENST00000445946.3:c.-780C= (KLLN) ENSP00000392204.2:n.-780C=
NM_001126049.1:c.-780C= (KLLN) NP_001119521.1:n.-780C=
NM_001126049.2:c.-780C= (KLLN) MANE Select NP_001119521.1:n.-780C=
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