Canonical Allele Identifier: CA891841564

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965320_87965321delinsGG , CM000672.2:g.87965320_87965321delinsGG	GRCh38
NC_000010.10:g.89725077_89725078delinsGG , CM000672.1:g.89725077_89725078delinsGG	GRCh37
NC_000010.9:g.89715057_89715058delinsGG	NCBI36
NG_007466.2:g.106882_106883delinsGG , LRG_311:g.106882_106883delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1153_1154delinsGG	ENSP00000514759.2:p.Pro385Gly
ENST00000710265.1:c.*89_*90delinsGG	ENSP00000518161.1:n.*89_*90delinsGG
ENST00000688158.2:n.1795_1796delinsGG
ENST00000688922.2:c.*890_*891delinsGG	ENSP00000508742.2:n.*890_*891delinsGG
ENST00000700021.1:c.1015_1016delinsGG	ENSP00000514757.1:p.Pro339Gly
ENST00000700022.1:c.*399_*400delinsGG	ENSP00000514758.1:n.*399_*400delinsGG
ENST00000700023.1:n.2218_2219delinsGG
ENST00000700024.1:n.2452_2453delinsGG
ENST00000706954.1:c.1060_1061delinsGG	ENSP00000516674.1:p.Pro354Gly
ENST00000706955.1:c.*1095_*1096delinsGG	ENSP00000516675.1:n.*1095_*1096delinsGG
ENST00000686459.1:c.*646_*647delinsGG	ENSP00000508909.1:n.*646_*647delinsGG
ENST00000688158.1:c.*1171_*1172delinsGG	ENSP00000509254.1:n.*1171_*1172delinsGG
ENST00000688308.1:c.1060_1061delinsGG	ENSP00000508752.1:p.Pro354Gly
ENST00000688922.1:c.981_982delinsGG
ENST00000693560.1:c.1579_1580delinsGG	ENSP00000509861.1:p.Pro527Gly
ENST00000371953.8:c.1060_1061delinsGG MANE Select	ENSP00000361021.3:p.Pro354Gly
ENST00000371953.7:c.1060_1061delinsGG	ENSP00000361021.3:p.Pro354Gly
NM_000314.5:c.1060_1061delinsGG	NP_000305.3:p.Pro354Gly
NM_000314.6:c.1060_1061delinsGG	NP_000305.3:p.Pro354Gly
NM_001304717.2:c.1579_1580delinsGG	NP_001291646.2:p.Pro527Gly
NM_001304718.1:c.469_470delinsGG	NP_001291647.1:p.Pro157Gly
XM_006717926.2:c.1015_1016delinsGG	XP_006717989.1:p.Pro339Gly
XM_011539982.1:c.964_965delinsGG	XP_011538284.1:p.Pro322Gly
XR_945791.1:n.1630_1631delinsGG
NM_000314.7:c.1060_1061delinsGG	NP_000305.3:p.Pro354Gly
NM_001304717.5:c.1579_1580delinsGG	NP_001291646.4:p.Pro527Gly
NM_001304718.2:c.469_470delinsGG	NP_001291647.1:p.Pro157Gly
NM_000314.8:c.1060_1061delinsGG MANE Select	NP_000305.3:p.Pro354Gly