Canonical Allele Identifier: CA645553772
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87931049_87933015del , CM000672.2:g.87931049_87933015del GRCh38
NC_000010.10:g.89690806_89692772del , CM000672.1:g.89690806_89692772del GRCh37
NC_000010.9:g.89680786_89682752del NCBI36
NG_007466.2:g.72611_74577del , LRG_311:g.72611_74577del

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.213_256del
ENST00000710265.1:c.213_256del
ENST00000472832.3:c.213_256del
ENST00000688158.2:n.948_991del
ENST00000688922.2:c.*43_*86del
ENST00000700021.1:c.168_211del
ENST00000700022.1:c.213_256del
ENST00000700029.1:c.47_90del
ENST00000706954.1:c.213_256del
ENST00000706955.1:c.*248_*291del
ENST00000686459.1:c.213_256del
ENST00000688158.1:c.*324_*367del
ENST00000688308.1:c.213_256del
ENST00000688922.1:c.134_177del
ENST00000693560.1:c.732_775del
ENST00000371953.8:c.213_256del
ENST00000371953.7:c.213_256del
ENST00000498703.1:n.39_82del
ENST00000610634.1:c.111_154del
NM_000314.5:c.213_256del
NM_000314.6:c.213_256del
NM_001304717.2:c.732_775del
NM_001304718.1:c.-538_-495del
XM_006717926.2:c.168_211del
XM_011539981.1:c.213_256del
XM_011539982.1:c.117_160del
XR_945789.1:n.925_968del
XR_945790.1:n.925_968del
XR_945791.1:n.925_968del
NM_000314.7:c.213_256del
NM_001304717.5:c.732_775del
NM_001304718.2:c.-538_-495del
NM_000314.8:c.213_256del