Canonical Allele Identifier: CA891841667

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965434_87965435delinsCC , CM000672.2:g.87965434_87965435delinsCC	GRCh38
NC_000010.10:g.89725191_89725192delinsCC , CM000672.1:g.89725191_89725192delinsCC	GRCh37
NC_000010.9:g.89715171_89715172delinsCC	NCBI36
NG_007466.2:g.106996_106997delinsCC , LRG_311:g.106996_106997delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1267_1268delinsCC	ENSP00000514759.2:p.Phe423Pro
ENST00000710265.1:c.*203_*204delinsCC	ENSP00000518161.1:n.*203_*204delinsCC
ENST00000688158.2:n.1909_1910delinsCC
ENST00000688922.2:c.*1004_*1005delinsCC	ENSP00000508742.2:n.*1004_*1005delinsCC
ENST00000700021.1:c.1129_1130delinsCC	ENSP00000514757.1:p.Phe377Pro
ENST00000700022.1:c.*513_*514delinsCC	ENSP00000514758.1:n.*513_*514delinsCC
ENST00000700023.1:n.2332_2333delinsCC
ENST00000700024.1:n.2566_2567delinsCC
ENST00000706954.1:c.1174_1175delinsCC	ENSP00000516674.1:p.Phe392Pro
ENST00000706955.1:c.*1209_*1210delinsCC	ENSP00000516675.1:n.*1209_*1210delinsCC
ENST00000686459.1:c.*760_*761delinsCC	ENSP00000508909.1:n.*760_*761delinsCC
ENST00000688158.1:c.*1285_*1286delinsCC	ENSP00000509254.1:n.*1285_*1286delinsCC
ENST00000688308.1:c.1174_1175delinsCC	ENSP00000508752.1:p.Phe392Pro
ENST00000688922.1:c.1095_1096delinsCC
ENST00000693560.1:c.1693_1694delinsCC	ENSP00000509861.1:p.Phe565Pro
ENST00000371953.8:c.1174_1175delinsCC MANE Select	ENSP00000361021.3:p.Phe392Pro
ENST00000371953.7:c.1174_1175delinsCC	ENSP00000361021.3:p.Phe392Pro
NM_000314.5:c.1174_1175delinsCC	NP_000305.3:p.Phe392Pro
NM_000314.6:c.1174_1175delinsCC	NP_000305.3:p.Phe392Pro
NM_001304717.2:c.1693_1694delinsCC	NP_001291646.2:p.Phe565Pro
NM_001304718.1:c.583_584delinsCC	NP_001291647.1:p.Phe195Pro
XM_006717926.2:c.1129_1130delinsCC	XP_006717989.1:p.Phe377Pro
XM_011539982.1:c.1078_1079delinsCC	XP_011538284.1:p.Phe360Pro
XR_945791.1:n.1744_1745delinsCC
NM_000314.7:c.1174_1175delinsCC	NP_000305.3:p.Phe392Pro
NM_001304717.5:c.1693_1694delinsCC	NP_001291646.4:p.Phe565Pro
NM_001304718.2:c.583_584delinsCC	NP_001291647.1:p.Phe195Pro
NM_000314.8:c.1174_1175delinsCC MANE Select	NP_000305.3:p.Phe392Pro