Canonical Allele Identifier: CA891837347

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965339_87965340delinsTT , CM000672.2:g.87965339_87965340delinsTT	GRCh38
NC_000010.10:g.89725096_89725097delinsTT , CM000672.1:g.89725096_89725097delinsTT	GRCh37
NC_000010.9:g.89715076_89715077delinsTT	NCBI36
NG_007466.2:g.106901_106902delinsTT , LRG_311:g.106901_106902delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1172_1173delinsTT	ENSP00000514759.2:p.Ser391Ile
ENST00000710265.1:c.*108_*109delinsTT	ENSP00000518161.1:n.*108_*109delinsTT
ENST00000688158.2:n.1814_1815delinsTT
ENST00000688922.2:c.*909_*910delinsTT	ENSP00000508742.2:n.*909_*910delinsTT
ENST00000700021.1:c.1034_1035delinsTT	ENSP00000514757.1:p.Ser345Ile
ENST00000700022.1:c.*418_*419delinsTT	ENSP00000514758.1:n.*418_*419delinsTT
ENST00000700023.1:n.2237_2238delinsTT
ENST00000700024.1:n.2471_2472delinsTT
ENST00000706954.1:c.1079_1080delinsTT	ENSP00000516674.1:p.Ser360Ile
ENST00000706955.1:c.*1114_*1115delinsTT	ENSP00000516675.1:n.*1114_*1115delinsTT
ENST00000686459.1:c.*665_*666delinsTT	ENSP00000508909.1:n.*665_*666delinsTT
ENST00000688158.1:c.*1190_*1191delinsTT	ENSP00000509254.1:n.*1190_*1191delinsTT
ENST00000688308.1:c.1079_1080delinsTT	ENSP00000508752.1:p.Ser360Ile
ENST00000688922.1:c.1000_1001delinsTT
ENST00000693560.1:c.1598_1599delinsTT	ENSP00000509861.1:p.Ser533Ile
ENST00000371953.8:c.1079_1080delinsTT MANE Select	ENSP00000361021.3:p.Ser360Ile
ENST00000371953.7:c.1079_1080delinsTT	ENSP00000361021.3:p.Ser360Ile
NM_000314.5:c.1079_1080delinsTT	NP_000305.3:p.Ser360Ile
NM_000314.6:c.1079_1080delinsTT	NP_000305.3:p.Ser360Ile
NM_001304717.2:c.1598_1599delinsTT	NP_001291646.2:p.Ser533Ile
NM_001304718.1:c.488_489delinsTT	NP_001291647.1:p.Ser163Ile
XM_006717926.2:c.1034_1035delinsTT	XP_006717989.1:p.Ser345Ile
XM_011539982.1:c.983_984delinsTT	XP_011538284.1:p.Ser328Ile
XR_945791.1:n.1649_1650delinsTT
NM_000314.7:c.1079_1080delinsTT	NP_000305.3:p.Ser360Ile
NM_001304717.5:c.1598_1599delinsTT	NP_001291646.4:p.Ser533Ile
NM_001304718.2:c.488_489delinsTT	NP_001291647.1:p.Ser163Ile
NM_000314.8:c.1079_1080delinsTT MANE Select	NP_000305.3:p.Ser360Ile