Canonical Allele Identifier: CA2832602930

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961111_87961128del , CM000672.2:g.87961111_87961128del	GRCh38
NC_000010.10:g.89720868_89720885del , CM000672.1:g.89720868_89720885del	GRCh37
NC_000010.9:g.89710848_89710865del	NCBI36
NG_007466.2:g.102673_102690del , LRG_311:g.102673_102690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1112_1119+10del
ENST00000710265.1:c.1019_1026+10del
ENST00000472832.3:c.1019_*1del	ENSP00000483066.2:n.[c.1019_*1del;Asn340IlefsTer?]
ENST00000688158.2:n.1754_1761+10del
ENST00000688922.2:c.*849_*856+10del
ENST00000700021.1:c.974_981+10del
ENST00000700022.1:c.*358_*365+10del
ENST00000700023.1:n.2177_2184+10del
ENST00000700024.1:n.2411_2418+10del
ENST00000700025.1:n.1788_1805del
ENST00000700026.1:n.656_673del
ENST00000706954.1:c.1019_1026+10del
ENST00000706955.1:c.*1054_*1061+10del
ENST00000686459.1:c.*605_*612+10del
ENST00000688158.1:c.*1130_*1137+10del
ENST00000688308.1:c.1019_1026+10del
ENST00000688922.1:c.940_947+10del
ENST00000693560.1:c.1538_1545+10del
ENST00000371953.8:c.1019_1026+10del
ENST00000371953.7:c.1019_1026+10del
ENST00000472832.2:c.446_463del	ENSP00000483066.1:n.[c.446_463del;Asn149IlefsTer?]
NM_000314.5:c.1019_1026+10del
NM_000314.6:c.1019_1026+10del
NM_001304717.2:c.1538_1545+10del
NM_001304718.1:c.428_435+10del
XM_006717926.2:c.974_981+10del
XM_011539981.1:c.1019_1026+10del
XM_011539982.1:c.923_930+10del
XR_945791.1:n.1589_1596+10del
NM_000314.7:c.1019_1026+10del
NM_001304717.5:c.1538_1545+10del
NM_001304718.2:c.428_435+10del
NM_000314.8:c.1019_1026+10del