Canonical Allele Identifier: CA891835256

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960964_87960965delinsTT , CM000672.2:g.87960964_87960965delinsTT	GRCh38
NC_000010.10:g.89720721_89720722delinsTT , CM000672.1:g.89720721_89720722delinsTT	GRCh37
NC_000010.9:g.89710701_89710702delinsTT	NCBI36
NG_007466.2:g.102526_102527delinsTT , LRG_311:g.102526_102527delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.965_966delinsTT	ENSP00000514759.2:p.Glu322Val
ENST00000710265.1:c.872_873delinsTT	ENSP00000518161.1:p.Glu291Val
ENST00000472832.3:c.872_873delinsTT	ENSP00000483066.2:p.Glu291Val
ENST00000688158.2:n.1607_1608delinsTT
ENST00000688922.2:c.*702_*703delinsTT	ENSP00000508742.2:n.*702_*703delinsTT
ENST00000700021.1:c.827_828delinsTT	ENSP00000514757.1:p.Glu276Val
ENST00000700022.1:c.*211_*212delinsTT	ENSP00000514758.1:n.*211_*212delinsTT
ENST00000700023.1:n.2030_2031delinsTT
ENST00000700024.1:n.2264_2265delinsTT
ENST00000700025.1:n.1641_1642delinsTT
ENST00000700026.1:n.509_510delinsTT
ENST00000700029.1:c.799_800delinsTT
ENST00000706954.1:c.872_873delinsTT	ENSP00000516674.1:p.Glu291Val
ENST00000706955.1:c.*907_*908delinsTT	ENSP00000516675.1:n.*907_*908delinsTT
ENST00000686459.1:c.*458_*459delinsTT	ENSP00000508909.1:n.*458_*459delinsTT
ENST00000688158.1:c.*983_*984delinsTT	ENSP00000509254.1:n.*983_*984delinsTT
ENST00000688308.1:c.872_873delinsTT	ENSP00000508752.1:p.Glu291Val
ENST00000688922.1:c.793_794delinsTT
ENST00000693560.1:c.1391_1392delinsTT	ENSP00000509861.1:p.Glu464Val
ENST00000371953.8:c.872_873delinsTT MANE Select	ENSP00000361021.3:p.Glu291Val
ENST00000371953.7:c.872_873delinsTT	ENSP00000361021.3:p.Glu291Val
ENST00000472832.2:c.299_300delinsTT	ENSP00000483066.1:p.Glu100Val
NM_000314.5:c.872_873delinsTT	NP_000305.3:p.Glu291Val
NM_000314.6:c.872_873delinsTT	NP_000305.3:p.Glu291Val
NM_001304717.2:c.1391_1392delinsTT	NP_001291646.2:p.Glu464Val
NM_001304718.1:c.281_282delinsTT	NP_001291647.1:p.Glu94Val
XM_006717926.2:c.827_828delinsTT	XP_006717989.1:p.Glu276Val
XM_011539981.1:c.872_873delinsTT	XP_011538283.1:p.Glu291Val
XM_011539982.1:c.776_777delinsTT	XP_011538284.1:p.Glu259Val
XR_945791.1:n.1442_1443delinsTT
NM_000314.7:c.872_873delinsTT	NP_000305.3:p.Glu291Val
NM_001304717.5:c.1391_1392delinsTT	NP_001291646.4:p.Glu464Val
NM_001304718.2:c.281_282delinsTT	NP_001291647.1:p.Glu94Val
NM_000314.8:c.872_873delinsTT MANE Select	NP_000305.3:p.Glu291Val