Canonical Allele Identifier: CA2610046150
Gene: PTEN HGNC NCBI
KLLN HGNC NCBI

Linked Data

gnomAD v4: 10-87863435-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863436del , CM000672.2:g.87863436del GRCh38
NC_000010.10:g.89623193del , CM000672.1:g.89623193del GRCh37
NC_000010.9:g.89613173del NCBI36
NG_007466.2:g.4999del , LRG_311:g.4999del
NG_033079.1:g.5002del

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+794del (PTEN) ENSP00000516674.1:n.-17+794del
ENST00000688308.1:c.-17+323del (PTEN) ENSP00000508752.1:n.-17+323del
ENST00000445946.5:c.-949del (KLLN) MANE Select ENSP00000392204.2:n.-949del
ENST00000371953.7:c.-1034del (PTEN) ENSP00000361021.3:n.-1034del
ENST00000445946.3:c.-949del (KLLN) ENSP00000392204.2:n.-949del
NM_001126049.1:c.-949del (KLLN) NP_001119521.1:n.-949del
NM_001126049.2:c.-949del (KLLN) MANE Select NP_001119521.1:n.-949del
Search 100 bp 5'
Search 100 bp 3'