Canonical Allele Identifier: CA891838180

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965449_87965451delinsTAA , CM000672.2:g.87965449_87965451delinsTAA	GRCh38
NC_000010.10:g.89725206_89725208delinsTAA , CM000672.1:g.89725206_89725208delinsTAA	GRCh37
NC_000010.9:g.89715186_89715188delinsTAA	NCBI36
NG_007466.2:g.107011_107013delinsTAA , LRG_311:g.107011_107013delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1282_1284delinsTAA	ENSP00000514759.2:p.His428Ter
ENST00000710265.1:c.*218_*220delinsTAA	ENSP00000518161.1:n.*218_*220delinsTAA
ENST00000688158.2:n.1924_1926delinsTAA
ENST00000688922.2:c.*1019_*1021delinsTAA	ENSP00000508742.2:n.*1019_*1021delinsTAA
ENST00000700021.1:c.1144_1146delinsTAA	ENSP00000514757.1:p.His382Ter
ENST00000700022.1:c.*528_*530delinsTAA	ENSP00000514758.1:n.*528_*530delinsTAA
ENST00000700023.1:n.2347_2349delinsTAA
ENST00000700024.1:n.2581_2583delinsTAA
ENST00000706954.1:c.1189_1191delinsTAA	ENSP00000516674.1:p.His397Ter
ENST00000706955.1:c.*1224_*1226delinsTAA	ENSP00000516675.1:n.*1224_*1226delinsTAA
ENST00000686459.1:c.*775_*777delinsTAA	ENSP00000508909.1:n.*775_*777delinsTAA
ENST00000688158.1:c.*1300_*1302delinsTAA	ENSP00000509254.1:n.*1300_*1302delinsTAA
ENST00000688308.1:c.1189_1191delinsTAA	ENSP00000508752.1:p.His397Ter
ENST00000688922.1:c.1110_1112delinsTAA
ENST00000693560.1:c.1708_1710delinsTAA	ENSP00000509861.1:p.His570Ter
ENST00000371953.8:c.1189_1191delinsTAA MANE Select	ENSP00000361021.3:p.His397Ter
ENST00000371953.7:c.1189_1191delinsTAA	ENSP00000361021.3:p.His397Ter
NM_000314.5:c.1189_1191delinsTAA	NP_000305.3:p.His397Ter
NM_000314.6:c.1189_1191delinsTAA	NP_000305.3:p.His397Ter
NM_001304717.2:c.1708_1710delinsTAA	NP_001291646.2:p.His570Ter
NM_001304718.1:c.598_600delinsTAA	NP_001291647.1:p.His200Ter
XM_006717926.2:c.1144_1146delinsTAA	XP_006717989.1:p.His382Ter
XM_011539982.1:c.1093_1095delinsTAA	XP_011538284.1:p.His365Ter
XR_945791.1:n.1759_1761delinsTAA
NM_000314.7:c.1189_1191delinsTAA	NP_000305.3:p.His397Ter
NM_001304717.5:c.1708_1710delinsTAA	NP_001291646.4:p.His570Ter
NM_001304718.2:c.598_600delinsTAA	NP_001291647.1:p.His200Ter
NM_000314.8:c.1189_1191delinsTAA MANE Select	NP_000305.3:p.His397Ter