Canonical Allele Identifier: CA1926142828
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863265T= , CM000672.2:g.87863265T= GRCh38
NC_000010.10:g.89623022T= , CM000672.1:g.89623022T= GRCh37
NC_000010.9:g.89613002T= NCBI36
NG_007466.2:g.4828T= , LRG_311:g.4828T=
NG_033079.1:g.5173A=

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+623T= (PTEN) ENSP00000516674.1:n.-17+623T=
ENST00000688308.1:c.-17+152T= (PTEN) ENSP00000508752.1:n.-17+152T=
ENST00000445946.5:c.-778A= (KLLN) MANE Select ENSP00000392204.2:n.-778A=
ENST00000371953.7:c.-1205T= (PTEN) ENSP00000361021.3:n.-1205T=
ENST00000445946.3:c.-778A= (KLLN) ENSP00000392204.2:n.-778A=
NM_001126049.1:c.-778A= (KLLN) NP_001119521.1:n.-778A=
NM_001126049.2:c.-778A= (KLLN) MANE Select NP_001119521.1:n.-778A=
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