Canonical Allele Identifier: CA891840731

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894108_87894109delinsGT , CM000672.2:g.87894108_87894109delinsGT	GRCh38
NC_000010.10:g.89653865_89653866delinsGT , CM000672.1:g.89653865_89653866delinsGT	GRCh37
NC_000010.9:g.89643845_89643846delinsGT	NCBI36
NG_007466.2:g.35670_35671delinsGT , LRG_311:g.35670_35671delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.163_164delinsGT	ENSP00000514759.2:p.Arg55Val
ENST00000710265.1:c.163_164delinsGT	ENSP00000518161.1:p.Arg55Val
ENST00000472832.3:c.163_164delinsGT	ENSP00000483066.2:p.Arg55Val
ENST00000688158.2:n.899+13670_899+13671delinsGT
ENST00000688922.2:c.163_164delinsGT	ENSP00000508742.2:p.Arg55Val
ENST00000700021.1:c.163_164delinsGT	ENSP00000514757.1:p.Ser55Val
ENST00000700022.1:c.163_164delinsGT	ENSP00000514758.1:p.Arg55Val
ENST00000706954.1:c.163_164delinsGT	ENSP00000516674.1:p.Arg55Val
ENST00000706955.1:c.*198_*199delinsGT	ENSP00000516675.1:n.*198_*199delinsGT
ENST00000686459.1:c.163_164delinsGT	ENSP00000508909.1:p.Arg55Val
ENST00000688158.1:c.*275+13670_*275+13671delinsGT	ENSP00000509254.1:n.*275+13670_*275+13671delinsGT
ENST00000688308.1:c.163_164delinsGT	ENSP00000508752.1:p.Arg55Val
ENST00000688922.1:c.32_33delinsGT
ENST00000693560.1:c.682_683delinsGT	ENSP00000509861.1:p.Arg228Val
ENST00000371953.8:c.163_164delinsGT MANE Select	ENSP00000361021.3:p.Arg55Val
ENST00000371953.7:c.163_164delinsGT	ENSP00000361021.3:p.Arg55Val
ENST00000462694.1:n.165_166delinsGT
ENST00000610634.1:c.61_62delinsGT	ENSP00000477517.1:p.Arg21Val
NM_000314.5:c.163_164delinsGT	NP_000305.3:p.Arg55Val
NM_000314.6:c.163_164delinsGT	NP_000305.3:p.Arg55Val
NM_001304717.2:c.682_683delinsGT	NP_001291646.2:p.Arg228Val
NM_001304718.1:c.-543_-542delinsGT	NP_001291647.1:n.-543_-542delinsGT
XM_006717926.2:c.163_164delinsGT	XP_006717989.1:p.Ser55Val
XM_011539981.1:c.163_164delinsGT	XP_011538283.1:p.Arg55Val
XM_011539982.1:c.68+13670_68+13671delinsGT	XP_011538284.1:n.68+13670_68+13671delinsGT
XR_945789.1:n.875_876delinsGT
XR_945790.1:n.875_876delinsGT
XR_945791.1:n.875_876delinsGT
NM_000314.7:c.163_164delinsGT	NP_000305.3:p.Arg55Val
NM_001304717.5:c.682_683delinsGT	NP_001291646.4:p.Arg228Val
NM_001304718.2:c.-543_-542delinsGT	NP_001291647.1:n.-543_-542delinsGT
NM_000314.8:c.163_164delinsGT MANE Select	NP_000305.3:p.Arg55Val