Canonical Allele Identifier: CA891836165

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961015_87961016delinsCA , CM000672.2:g.87961015_87961016delinsCA	GRCh38
NC_000010.10:g.89720772_89720773delinsCA , CM000672.1:g.89720772_89720773delinsCA	GRCh37
NC_000010.9:g.89710752_89710753delinsCA	NCBI36
NG_007466.2:g.102577_102578delinsCA , LRG_311:g.102577_102578delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1016_1017delinsCA	ENSP00000514759.2:p.Arg339Pro
ENST00000710265.1:c.923_924delinsCA	ENSP00000518161.1:p.Arg308Pro
ENST00000472832.3:c.923_924delinsCA	ENSP00000483066.2:p.Arg308Pro
ENST00000688158.2:n.1658_1659delinsCA
ENST00000688922.2:c.*753_*754delinsCA	ENSP00000508742.2:n.*753_*754delinsCA
ENST00000700021.1:c.878_879delinsCA	ENSP00000514757.1:p.Arg293Pro
ENST00000700022.1:c.*262_*263delinsCA	ENSP00000514758.1:n.*262_*263delinsCA
ENST00000700023.1:n.2081_2082delinsCA
ENST00000700024.1:n.2315_2316delinsCA
ENST00000700025.1:n.1692_1693delinsCA
ENST00000700026.1:n.560_561delinsCA
ENST00000706954.1:c.923_924delinsCA	ENSP00000516674.1:p.Arg308Pro
ENST00000706955.1:c.*958_*959delinsCA	ENSP00000516675.1:n.*958_*959delinsCA
ENST00000686459.1:c.*509_*510delinsCA	ENSP00000508909.1:n.*509_*510delinsCA
ENST00000688158.1:c.*1034_*1035delinsCA	ENSP00000509254.1:n.*1034_*1035delinsCA
ENST00000688308.1:c.923_924delinsCA	ENSP00000508752.1:p.Arg308Pro
ENST00000688922.1:c.844_845delinsCA
ENST00000693560.1:c.1442_1443delinsCA	ENSP00000509861.1:p.Arg481Pro
ENST00000371953.8:c.923_924delinsCA MANE Select	ENSP00000361021.3:p.Arg308Pro
ENST00000371953.7:c.923_924delinsCA	ENSP00000361021.3:p.Arg308Pro
ENST00000472832.2:c.350_351delinsCA	ENSP00000483066.1:p.Arg117Pro
NM_000314.5:c.923_924delinsCA	NP_000305.3:p.Arg308Pro
NM_000314.6:c.923_924delinsCA	NP_000305.3:p.Arg308Pro
NM_001304717.2:c.1442_1443delinsCA	NP_001291646.2:p.Arg481Pro
NM_001304718.1:c.332_333delinsCA	NP_001291647.1:p.Arg111Pro
XM_006717926.2:c.878_879delinsCA	XP_006717989.1:p.Arg293Pro
XM_011539981.1:c.923_924delinsCA	XP_011538283.1:p.Arg308Pro
XM_011539982.1:c.827_828delinsCA	XP_011538284.1:p.Arg276Pro
XR_945791.1:n.1493_1494delinsCA
NM_000314.7:c.923_924delinsCA	NP_000305.3:p.Arg308Pro
NM_001304717.5:c.1442_1443delinsCA	NP_001291646.4:p.Arg481Pro
NM_001304718.2:c.332_333delinsCA	NP_001291647.1:p.Arg111Pro
NM_000314.8:c.923_924delinsCA MANE Select	NP_000305.3:p.Arg308Pro