Canonical Allele Identifier: CA2610046361

Gene: PTEN

Linked Data

• gnomAD v4: 10-87863537-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863538del , CM000672.2:g.87863538del	GRCh38
NC_000010.10:g.89623295del , CM000672.1:g.89623295del	GRCh37
NC_000010.9:g.89613275del	NCBI36
NG_007466.2:g.5101del , LRG_311:g.5101del
NG_033079.1:g.4900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+896del	ENSP00000516674.1:n.-17+896del
ENST00000688308.1:c.-17+425del	ENSP00000508752.1:n.-17+425del
ENST00000693560.1:c.-412del	ENSP00000509861.1:n.-412del
ENST00000371953.7:c.-932del	ENSP00000361021.3:n.-932del
ENST00000610634.1:c.-1034del	ENSP00000477517.1:n.-1034del
NM_000314.5:c.-931del	NP_000305.3:n.-931del
NM_000314.6:c.-931del	NP_000305.3:n.-931del
NM_001304717.2:c.-412del	NP_001291646.2:n.-412del
NM_001304718.1:c.-1636del	NP_001291647.1:n.-1636del