Canonical Allele Identifier: CA891838061

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965429_87965430delinsGT , CM000672.2:g.87965429_87965430delinsGT	GRCh38
NC_000010.10:g.89725186_89725187delinsGT , CM000672.1:g.89725186_89725187delinsGT	GRCh37
NC_000010.9:g.89715166_89715167delinsGT	NCBI36
NG_007466.2:g.106991_106992delinsGT , LRG_311:g.106991_106992delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1262_1263delinsGT	ENSP00000514759.2:p.Glu421Gly
ENST00000710265.1:c.*198_*199delinsGT	ENSP00000518161.1:n.*198_*199delinsGT
ENST00000688158.2:n.1904_1905delinsGT
ENST00000688922.2:c.*999_*1000delinsGT	ENSP00000508742.2:n.*999_*1000delinsGT
ENST00000700021.1:c.1124_1125delinsGT	ENSP00000514757.1:p.Glu375Gly
ENST00000700022.1:c.*508_*509delinsGT	ENSP00000514758.1:n.*508_*509delinsGT
ENST00000700023.1:n.2327_2328delinsGT
ENST00000700024.1:n.2561_2562delinsGT
ENST00000706954.1:c.1169_1170delinsGT	ENSP00000516674.1:p.Glu390Gly
ENST00000706955.1:c.*1204_*1205delinsGT	ENSP00000516675.1:n.*1204_*1205delinsGT
ENST00000686459.1:c.*755_*756delinsGT	ENSP00000508909.1:n.*755_*756delinsGT
ENST00000688158.1:c.*1280_*1281delinsGT	ENSP00000509254.1:n.*1280_*1281delinsGT
ENST00000688308.1:c.1169_1170delinsGT	ENSP00000508752.1:p.Glu390Gly
ENST00000688922.1:c.1090_1091delinsGT
ENST00000693560.1:c.1688_1689delinsGT	ENSP00000509861.1:p.Glu563Gly
ENST00000371953.8:c.1169_1170delinsGT MANE Select	ENSP00000361021.3:p.Glu390Gly
ENST00000371953.7:c.1169_1170delinsGT	ENSP00000361021.3:p.Glu390Gly
NM_000314.5:c.1169_1170delinsGT	NP_000305.3:p.Glu390Gly
NM_000314.6:c.1169_1170delinsGT	NP_000305.3:p.Glu390Gly
NM_001304717.2:c.1688_1689delinsGT	NP_001291646.2:p.Glu563Gly
NM_001304718.1:c.578_579delinsGT	NP_001291647.1:p.Glu193Gly
XM_006717926.2:c.1124_1125delinsGT	XP_006717989.1:p.Glu375Gly
XM_011539982.1:c.1073_1074delinsGT	XP_011538284.1:p.Glu358Gly
XR_945791.1:n.1739_1740delinsGT
NM_000314.7:c.1169_1170delinsGT	NP_000305.3:p.Glu390Gly
NM_001304717.5:c.1688_1689delinsGT	NP_001291646.4:p.Glu563Gly
NM_001304718.2:c.578_579delinsGT	NP_001291647.1:p.Glu193Gly
NM_000314.8:c.1169_1170delinsGT MANE Select	NP_000305.3:p.Glu390Gly