Canonical Allele Identifier: CA595184727

Gene: PTEN

Linked Data

• ClinVar Variation Id: 2673888
• ClinVar RCV Id: RCV003450505
• dbSNP Id: rs1589665532
• gnomAD v2: 10-89720648-TAGGACAAAATGTTTCAC-T
• gnomAD v3: 10-87960891-TAGGACAAAATGTTTCAC-T
• gnomAD v4: 10-87960891-TAGGACAAAATGTTTCAC-T
• MyVariant Identifiers: chr10:g.89720649_89720665del (hg19) ; chr10:g.87960892_87960908del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960892_87960908del , CM000672.2:g.87960892_87960908del	GRCh38
NC_000010.10:g.89720649_89720665del , CM000672.1:g.89720649_89720665del	GRCh37
NC_000010.9:g.89710629_89710645del	NCBI36
NG_007466.2:g.102454_102470del , LRG_311:g.102454_102470del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-2_909del
ENST00000710265.1:c.802-2_816del
ENST00000472832.3:c.802-2_816del
ENST00000688158.2:n.1537-2_1551del
ENST00000688922.2:c.*632-2_*646del
ENST00000700021.1:c.757-2_771del
ENST00000700022.1:c.*141-2_*155del
ENST00000700023.1:n.1960-2_1974del
ENST00000700024.1:n.2194-2_2208del
ENST00000700025.1:n.1571-2_1585del
ENST00000700026.1:n.439-2_453del
ENST00000700029.1:c.729-2_743del
ENST00000706954.1:c.802-2_816del
ENST00000706955.1:c.*837-2_*851del
ENST00000686459.1:c.*388-2_*402del
ENST00000688158.1:c.*913-2_*927del
ENST00000688308.1:c.802-2_816del
ENST00000688922.1:c.723-2_737del
ENST00000693560.1:c.1321-2_1335del
ENST00000371953.8:c.802-2_816del
ENST00000371953.7:c.802-2_816del
ENST00000472832.2:c.229-2_243del
NM_000314.5:c.802-2_816del
NM_000314.6:c.802-2_816del
NM_001304717.2:c.1321-2_1335del
NM_001304718.1:c.211-2_225del
XM_006717926.2:c.757-2_771del
XM_011539981.1:c.802-2_816del
XM_011539982.1:c.706-2_720del
XR_945791.1:n.1372-2_1386del
NM_000314.7:c.802-2_816del
NM_001304717.5:c.1321-2_1335del
NM_001304718.2:c.211-2_225del
NM_000314.8:c.802-2_816del