Canonical Allele Identifier: CA2610045640

Gene: PTEN KLLN

Linked Data

• gnomAD v4: 10-87863153-C-CCATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863156_87863160dup , CM000672.2:g.87863156_87863160dup	GRCh38
NC_000010.10:g.89622913_89622917dup , CM000672.1:g.89622913_89622917dup	GRCh37
NC_000010.9:g.89612893_89612897dup	NCBI36
NG_007466.2:g.4719_4723dup , LRG_311:g.4719_4723dup
NG_033079.1:g.5280_5284dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+514_-17+518dup (PTEN)	ENSP00000516674.1:n.-17+514_-17+518dup
ENST00000688308.1:c.-17+43_-17+47dup (PTEN)	ENSP00000508752.1:n.-17+43_-17+47dup
ENST00000445946.5:c.-671_-667dup (KLLN) MANE Select	ENSP00000392204.2:n.-671_-667dup
ENST00000371953.7:c.-1314_-1310dup (PTEN)	ENSP00000361021.3:n.-1314_-1310dup
ENST00000445946.3:c.-671_-667dup (KLLN)	ENSP00000392204.2:n.-671_-667dup
NM_001126049.1:c.-671_-667dup (KLLN)	NP_001119521.1:n.-671_-667dup
NM_001126049.2:c.-671_-667dup (KLLN) MANE Select	NP_001119521.1:n.-671_-667dup