Canonical Allele Identifier: CA891841698

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965449_87965450delinsTC , CM000672.2:g.87965449_87965450delinsTC	GRCh38
NC_000010.10:g.89725206_89725207delinsTC , CM000672.1:g.89725206_89725207delinsTC	GRCh37
NC_000010.9:g.89715186_89715187delinsTC	NCBI36
NG_007466.2:g.107011_107012delinsTC , LRG_311:g.107011_107012delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1282_1283delinsTC	ENSP00000514759.2:p.His428Ser
ENST00000710265.1:c.*218_*219delinsTC	ENSP00000518161.1:n.*218_*219delinsTC
ENST00000688158.2:n.1924_1925delinsTC
ENST00000688922.2:c.*1019_*1020delinsTC	ENSP00000508742.2:n.*1019_*1020delinsTC
ENST00000700021.1:c.1144_1145delinsTC	ENSP00000514757.1:p.His382Ser
ENST00000700022.1:c.*528_*529delinsTC	ENSP00000514758.1:n.*528_*529delinsTC
ENST00000700023.1:n.2347_2348delinsTC
ENST00000700024.1:n.2581_2582delinsTC
ENST00000706954.1:c.1189_1190delinsTC	ENSP00000516674.1:p.His397Ser
ENST00000706955.1:c.*1224_*1225delinsTC	ENSP00000516675.1:n.*1224_*1225delinsTC
ENST00000686459.1:c.*775_*776delinsTC	ENSP00000508909.1:n.*775_*776delinsTC
ENST00000688158.1:c.*1300_*1301delinsTC	ENSP00000509254.1:n.*1300_*1301delinsTC
ENST00000688308.1:c.1189_1190delinsTC	ENSP00000508752.1:p.His397Ser
ENST00000688922.1:c.1110_1111delinsTC
ENST00000693560.1:c.1708_1709delinsTC	ENSP00000509861.1:p.His570Ser
ENST00000371953.8:c.1189_1190delinsTC MANE Select	ENSP00000361021.3:p.His397Ser
ENST00000371953.7:c.1189_1190delinsTC	ENSP00000361021.3:p.His397Ser
NM_000314.5:c.1189_1190delinsTC	NP_000305.3:p.His397Ser
NM_000314.6:c.1189_1190delinsTC	NP_000305.3:p.His397Ser
NM_001304717.2:c.1708_1709delinsTC	NP_001291646.2:p.His570Ser
NM_001304718.1:c.598_599delinsTC	NP_001291647.1:p.His200Ser
XM_006717926.2:c.1144_1145delinsTC	XP_006717989.1:p.His382Ser
XM_011539982.1:c.1093_1094delinsTC	XP_011538284.1:p.His365Ser
XR_945791.1:n.1759_1760delinsTC
NM_000314.7:c.1189_1190delinsTC	NP_000305.3:p.His397Ser
NM_001304717.5:c.1708_1709delinsTC	NP_001291646.4:p.His570Ser
NM_001304718.2:c.598_599delinsTC	NP_001291647.1:p.His200Ser
NM_000314.8:c.1189_1190delinsTC MANE Select	NP_000305.3:p.His397Ser