Canonical Allele Identifier: CA891834952

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925535_87925537delinsCAA , CM000672.2:g.87925535_87925537delinsCAA	GRCh38
NC_000010.10:g.89685292_89685294delinsCAA , CM000672.1:g.89685292_89685294delinsCAA	GRCh37
NC_000010.9:g.89675272_89675274delinsCAA	NCBI36
NG_007466.2:g.67097_67099delinsCAA , LRG_311:g.67097_67099delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.187_189delinsCAA	ENSP00000514759.2:p.Asn63Gln
ENST00000710265.1:c.187_189delinsCAA	ENSP00000518161.1:p.Asn63Gln
ENST00000472832.3:c.187_189delinsCAA	ENSP00000483066.2:p.Asn63Gln
ENST00000688158.2:n.922_924delinsCAA
ENST00000688922.2:c.187_189delinsCAA	ENSP00000508742.2:p.Asn63Gln
ENST00000700021.1:c.165-5511_165-5509delinsCAA	ENSP00000514757.1:n.165-5511_165-5509delinsCAA
ENST00000700022.1:c.187_189delinsCAA	ENSP00000514758.1:p.Asn63Gln
ENST00000700029.1:c.21_23delinsCAA
ENST00000706954.1:c.187_189delinsCAA	ENSP00000516674.1:p.Asn63Gln
ENST00000706955.1:c.*222_*224delinsCAA	ENSP00000516675.1:n.*222_*224delinsCAA
ENST00000686459.1:c.187_189delinsCAA	ENSP00000508909.1:p.Asn63Gln
ENST00000688158.1:c.*298_*300delinsCAA	ENSP00000509254.1:n.*298_*300delinsCAA
ENST00000688308.1:c.187_189delinsCAA	ENSP00000508752.1:p.Asn63Gln
ENST00000688922.1:c.56_58delinsCAA
ENST00000693560.1:c.706_708delinsCAA	ENSP00000509861.1:p.Asn236Gln
ENST00000371953.8:c.187_189delinsCAA MANE Select	ENSP00000361021.3:p.Asn63Gln
ENST00000371953.7:c.187_189delinsCAA	ENSP00000361021.3:p.Asn63Gln
ENST00000498703.1:n.13_15delinsCAA
ENST00000610634.1:c.85_87delinsCAA	ENSP00000477517.1:p.Asn29Gln
NM_000314.5:c.187_189delinsCAA	NP_000305.3:p.Asn63Gln
NM_000314.6:c.187_189delinsCAA	NP_000305.3:p.Asn63Gln
NM_001304717.2:c.706_708delinsCAA	NP_001291646.2:p.Asn236Gln
NM_001304718.1:c.-541-5511_-541-5509delinsCAA	NP_001291647.1:n.-541-5511_-541-5509delinsCAA
XM_006717926.2:c.165-5511_165-5509delinsCAA	XP_006717989.1:n.165-5511_165-5509delinsCAA
XM_011539981.1:c.187_189delinsCAA	XP_011538283.1:p.Asn63Gln
XM_011539982.1:c.91_93delinsCAA	XP_011538284.1:p.Asn31Gln
XR_945789.1:n.899_901delinsCAA
XR_945790.1:n.899_901delinsCAA
XR_945791.1:n.899_901delinsCAA
NM_000314.7:c.187_189delinsCAA	NP_000305.3:p.Asn63Gln
NM_001304717.5:c.706_708delinsCAA	NP_001291646.4:p.Asn236Gln
NM_001304718.2:c.-541-5511_-541-5509delinsCAA	NP_001291647.1:n.-541-5511_-541-5509delinsCAA
NM_000314.8:c.187_189delinsCAA MANE Select	NP_000305.3:p.Asn63Gln