Canonical Allele Identifier: CA891836845

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961077_87961078delinsGT , CM000672.2:g.87961077_87961078delinsGT	GRCh38
NC_000010.10:g.89720834_89720835delinsGT , CM000672.1:g.89720834_89720835delinsGT	GRCh37
NC_000010.9:g.89710814_89710815delinsGT	NCBI36
NG_007466.2:g.102639_102640delinsGT , LRG_311:g.102639_102640delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1078_1079delinsGT	ENSP00000514759.2:p.Asn360Val
ENST00000710265.1:c.985_986delinsGT	ENSP00000518161.1:p.Asn329Val
ENST00000472832.3:c.985_986delinsGT	ENSP00000483066.2:p.Asn329Val
ENST00000688158.2:n.1720_1721delinsGT
ENST00000688922.2:c.*815_*816delinsGT	ENSP00000508742.2:n.*815_*816delinsGT
ENST00000700021.1:c.940_941delinsGT	ENSP00000514757.1:p.Asn314Val
ENST00000700022.1:c.*324_*325delinsGT	ENSP00000514758.1:n.*324_*325delinsGT
ENST00000700023.1:n.2143_2144delinsGT
ENST00000700024.1:n.2377_2378delinsGT
ENST00000700025.1:n.1754_1755delinsGT
ENST00000700026.1:n.622_623delinsGT
ENST00000706954.1:c.985_986delinsGT	ENSP00000516674.1:p.Asn329Val
ENST00000706955.1:c.*1020_*1021delinsGT	ENSP00000516675.1:n.*1020_*1021delinsGT
ENST00000686459.1:c.*571_*572delinsGT	ENSP00000508909.1:n.*571_*572delinsGT
ENST00000688158.1:c.*1096_*1097delinsGT	ENSP00000509254.1:n.*1096_*1097delinsGT
ENST00000688308.1:c.985_986delinsGT	ENSP00000508752.1:p.Asn329Val
ENST00000688922.1:c.906_907delinsGT
ENST00000693560.1:c.1504_1505delinsGT	ENSP00000509861.1:p.Asn502Val
ENST00000371953.8:c.985_986delinsGT MANE Select	ENSP00000361021.3:p.Asn329Val
ENST00000371953.7:c.985_986delinsGT	ENSP00000361021.3:p.Asn329Val
ENST00000472832.2:c.412_413delinsGT	ENSP00000483066.1:p.Asn138Val
NM_000314.5:c.985_986delinsGT	NP_000305.3:p.Asn329Val
NM_000314.6:c.985_986delinsGT	NP_000305.3:p.Asn329Val
NM_001304717.2:c.1504_1505delinsGT	NP_001291646.2:p.Asn502Val
NM_001304718.1:c.394_395delinsGT	NP_001291647.1:p.Asn132Val
XM_006717926.2:c.940_941delinsGT	XP_006717989.1:p.Asn314Val
XM_011539981.1:c.985_986delinsGT	XP_011538283.1:p.Asn329Val
XM_011539982.1:c.889_890delinsGT	XP_011538284.1:p.Asn297Val
XR_945791.1:n.1555_1556delinsGT
NM_000314.7:c.985_986delinsGT	NP_000305.3:p.Asn329Val
NM_001304717.5:c.1504_1505delinsGT	NP_001291646.4:p.Asn502Val
NM_001304718.2:c.394_395delinsGT	NP_001291647.1:p.Asn132Val
NM_000314.8:c.985_986delinsGT MANE Select	NP_000305.3:p.Asn329Val