Canonical Allele Identifier: CA2722436838

Gene: PTEN

Linked Data

• dbSNP Id: rs2132187787

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894100_87894101del , CM000672.2:g.87894100_87894101del	GRCh38
NC_000010.10:g.89653857_89653858del , CM000672.1:g.89653857_89653858del	GRCh37
NC_000010.9:g.89643837_89643838del	NCBI36
NG_007466.2:g.35662_35663del , LRG_311:g.35662_35663del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.155_156del	ENSP00000514759.2:p.Asp52GlyfsTer10
ENST00000710265.1:c.155_156del	ENSP00000518161.1:p.Asp52GlyfsTer10
ENST00000472832.3:c.155_156del	ENSP00000483066.2:p.Asp52GlyfsTer10
ENST00000688158.2:n.899+13662_899+13663del
ENST00000688922.2:c.155_156del	ENSP00000508742.2:p.Asp52GlyfsTer10
ENST00000700021.1:c.155_156del	ENSP00000514757.1:p.Asp52GlyfsTer6
ENST00000700022.1:c.155_156del	ENSP00000514758.1:p.Asp52GlyfsTer10
ENST00000706954.1:c.155_156del	ENSP00000516674.1:p.Asp52GlyfsTer10
ENST00000706955.1:c.*190_*191del	ENSP00000516675.1:n.*190_*191del
ENST00000686459.1:c.155_156del	ENSP00000508909.1:p.Asp52GlyfsTer10
ENST00000688158.1:c.*275+13662_*275+13663del	ENSP00000509254.1:n.*275+13662_*275+13663del
ENST00000688308.1:c.155_156del	ENSP00000508752.1:p.Asp52GlyfsTer10
ENST00000688922.1:c.24_25del
ENST00000693560.1:c.674_675del	ENSP00000509861.1:p.Asp225GlyfsTer10
ENST00000371953.8:c.155_156del MANE Select	ENSP00000361021.3:p.Asp52GlyfsTer10
ENST00000371953.7:c.155_156del	ENSP00000361021.3:p.Asp52GlyfsTer10
ENST00000462694.1:n.157_158del
ENST00000610634.1:c.53_54del	ENSP00000477517.1:p.Asp18GlyfsTer10
NM_000314.5:c.155_156del	NP_000305.3:p.Asp52GlyfsTer10
NM_000314.6:c.155_156del	NP_000305.3:p.Asp52GlyfsTer10
NM_001304717.2:c.674_675del	NP_001291646.2:p.Asp225GlyfsTer10
NM_001304718.1:c.-551_-550del	NP_001291647.1:n.-551_-550del
XM_006717926.2:c.155_156del	XP_006717989.1:p.Asp52GlyfsTer6
XM_011539981.1:c.155_156del	XP_011538283.1:p.Asp52GlyfsTer10
XM_011539982.1:c.68+13662_68+13663del	XP_011538284.1:n.68+13662_68+13663del
XR_945789.1:n.867_868del
XR_945790.1:n.867_868del
XR_945791.1:n.867_868del
NM_000314.7:c.155_156del	NP_000305.3:p.Asp52GlyfsTer10
NM_001304717.5:c.674_675del	NP_001291646.4:p.Asp225GlyfsTer10
NM_001304718.2:c.-551_-550del	NP_001291647.1:n.-551_-550del
NM_000314.8:c.155_156del MANE Select	NP_000305.3:p.Asp52GlyfsTer10