Canonical Allele Identifier: CA2610046357

Gene: PTEN

Linked Data

• gnomAD v4: 10-87863532-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87863537del , CM000672.2:g.87863537del	GRCh38
NC_000010.10:g.89623294del , CM000672.1:g.89623294del	GRCh37
NC_000010.9:g.89613274del	NCBI36
NG_007466.2:g.5100del , LRG_311:g.5100del
NG_033079.1:g.4905del

Transcript Alleles

HGVS	Amino-acid change
ENST00000706954.1:c.-17+895del	ENSP00000516674.1:n.-17+895del
ENST00000688308.1:c.-17+424del	ENSP00000508752.1:n.-17+424del
ENST00000693560.1:c.-413del	ENSP00000509861.1:n.-413del
ENST00000371953.7:c.-933del	ENSP00000361021.3:n.-933del
ENST00000610634.1:c.-1035del	ENSP00000477517.1:n.-1035del
NM_000314.5:c.-932del	NP_000305.3:n.-932del
NM_000314.6:c.-932del	NP_000305.3:n.-932del
NM_001304717.2:c.-413del	NP_001291646.2:n.-413del
NM_001304718.1:c.-1637del	NP_001291647.1:n.-1637del