Canonical Allele Identifier: CA891834664

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925514_87925515delinsAA , CM000672.2:g.87925514_87925515delinsAA	GRCh38
NC_000010.10:g.89685271_89685272delinsAA , CM000672.1:g.89685271_89685272delinsAA	GRCh37
NC_000010.9:g.89675251_89675252delinsAA	NCBI36
NG_007466.2:g.67076_67077delinsAA , LRG_311:g.67076_67077delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.166_167delinsAA	ENSP00000514759.2:p.Phe56Asn
ENST00000710265.1:c.166_167delinsAA	ENSP00000518161.1:p.Phe56Asn
ENST00000472832.3:c.166_167delinsAA	ENSP00000483066.2:p.Phe56Asn
ENST00000688158.2:n.901_902delinsAA
ENST00000688922.2:c.166_167delinsAA	ENSP00000508742.2:p.Phe56Asn
ENST00000700021.1:c.165-5532_165-5531delinsAA	ENSP00000514757.1:n.165-5532_165-5531delinsAA
ENST00000700022.1:c.166_167delinsAA	ENSP00000514758.1:p.Phe56Asn
ENST00000706954.1:c.166_167delinsAA	ENSP00000516674.1:p.Phe56Asn
ENST00000706955.1:c.*201_*202delinsAA	ENSP00000516675.1:n.*201_*202delinsAA
ENST00000686459.1:c.166_167delinsAA	ENSP00000508909.1:p.Phe56Asn
ENST00000688158.1:c.*277_*278delinsAA	ENSP00000509254.1:n.*277_*278delinsAA
ENST00000688308.1:c.166_167delinsAA	ENSP00000508752.1:p.Phe56Asn
ENST00000688922.1:c.35_36delinsAA
ENST00000693560.1:c.685_686delinsAA	ENSP00000509861.1:p.Phe229Asn
ENST00000371953.8:c.166_167delinsAA MANE Select	ENSP00000361021.3:p.Phe56Asn
ENST00000371953.7:c.166_167delinsAA	ENSP00000361021.3:p.Phe56Asn
ENST00000610634.1:c.64_65delinsAA	ENSP00000477517.1:p.Phe22Asn
NM_000314.5:c.166_167delinsAA	NP_000305.3:p.Phe56Asn
NM_000314.6:c.166_167delinsAA	NP_000305.3:p.Phe56Asn
NM_001304717.2:c.685_686delinsAA	NP_001291646.2:p.Phe229Asn
NM_001304718.1:c.-541-5532_-541-5531delinsAA	NP_001291647.1:n.-541-5532_-541-5531delinsAA
XM_006717926.2:c.165-5532_165-5531delinsAA	XP_006717989.1:n.165-5532_165-5531delinsAA
XM_011539981.1:c.166_167delinsAA	XP_011538283.1:p.Phe56Asn
XM_011539982.1:c.70_71delinsAA	XP_011538284.1:p.Phe24Asn
XR_945789.1:n.878_879delinsAA
XR_945790.1:n.878_879delinsAA
XR_945791.1:n.878_879delinsAA
NM_000314.7:c.166_167delinsAA	NP_000305.3:p.Phe56Asn
NM_001304717.5:c.685_686delinsAA	NP_001291646.4:p.Phe229Asn
NM_001304718.2:c.-541-5532_-541-5531delinsAA	NP_001291647.1:n.-541-5532_-541-5531delinsAA
NM_000314.8:c.166_167delinsAA MANE Select	NP_000305.3:p.Phe56Asn