Canonical Allele Identifier: CA2610045269
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

gnomAD v4: 10-87863020-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863020C>A , CM000672.2:g.87863020C>A GRCh38
NC_000010.10:g.89622777C>A , CM000672.1:g.89622777C>A GRCh37
NC_000010.9:g.89612757C>A NCBI36
NG_007466.2:g.4583C>A , LRG_311:g.4583C>A
NG_033079.1:g.5418G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+378C>A (PTEN) ENSP00000516674.1:n.-17+378C>A
ENST00000688308.1:c.-110C>A (PTEN) ENSP00000508752.1:n.-110C>A
ENST00000445946.5:c.-533G>T (KLLN) MANE Select ENSP00000392204.2:n.-533G>T
ENST00000445946.3:c.-533G>T (KLLN) ENSP00000392204.2:n.-533G>T
NM_001126049.1:c.-533G>T (KLLN) NP_001119521.1:n.-533G>T
NM_001126049.2:c.-533G>T (KLLN) MANE Select NP_001119521.1:n.-533G>T
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