Canonical Allele Identifier: CA1926162899

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925542_87925543delinsAC , CM000672.2:g.87925542_87925543delinsAC	GRCh38
NC_000010.10:g.89685299_89685300delinsAC , CM000672.1:g.89685299_89685300delinsAC	GRCh37
NC_000010.9:g.89675279_89675280delinsAC	NCBI36
NG_007466.2:g.67104_67105delinsAC , LRG_311:g.67104_67105delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.194_195delinsAC	ENSP00000514759.2:p.Tyr65=
ENST00000710265.1:c.194_195delinsAC	ENSP00000518161.1:p.Tyr65=
ENST00000472832.3:c.194_195delinsAC	ENSP00000483066.2:p.Tyr65=
ENST00000688158.2:n.929_930delinsAC
ENST00000688922.2:c.194_195delinsAC	ENSP00000508742.2:p.Tyr65=
ENST00000700021.1:c.165-5504_165-5503delinsAC	ENSP00000514757.1:n.165-5504_165-5503delinsAC
ENST00000700022.1:c.194_195delinsAC	ENSP00000514758.1:p.Tyr65=
ENST00000700029.1:c.28_29delinsAC
ENST00000706954.1:c.194_195delinsAC	ENSP00000516674.1:p.Tyr65=
ENST00000706955.1:c.*229_*230delinsAC	ENSP00000516675.1:n.*229_*230delinsAC
ENST00000686459.1:c.194_195delinsAC	ENSP00000508909.1:p.Tyr65=
ENST00000688158.1:c.*305_*306delinsAC	ENSP00000509254.1:n.*305_*306delinsAC
ENST00000688308.1:c.194_195delinsAC	ENSP00000508752.1:p.Tyr65=
ENST00000688922.1:c.63_64delinsAC
ENST00000693560.1:c.713_714delinsAC	ENSP00000509861.1:p.Tyr238=
ENST00000371953.8:c.194_195delinsAC MANE Select	ENSP00000361021.3:p.Tyr65=
ENST00000371953.7:c.194_195delinsAC	ENSP00000361021.3:p.Tyr65=
ENST00000498703.1:n.20_21delinsAC
ENST00000610634.1:c.92_93delinsAC	ENSP00000477517.1:p.Tyr31=
NM_000314.5:c.194_195delinsAC	NP_000305.3:p.Tyr65=
NM_000314.6:c.194_195delinsAC	NP_000305.3:p.Tyr65=
NM_001304717.2:c.713_714delinsAC	NP_001291646.2:p.Tyr238=
NM_001304718.1:c.-541-5504_-541-5503delinsAC	NP_001291647.1:n.-541-5504_-541-5503delinsAC
XM_006717926.2:c.165-5504_165-5503delinsAC	XP_006717989.1:n.165-5504_165-5503delinsAC
XM_011539981.1:c.194_195delinsAC	XP_011538283.1:p.Tyr65=
XM_011539982.1:c.98_99delinsAC	XP_011538284.1:p.Tyr33=
XR_945789.1:n.906_907delinsAC
XR_945790.1:n.906_907delinsAC
XR_945791.1:n.906_907delinsAC
NM_000314.7:c.194_195delinsAC	NP_000305.3:p.Tyr65=
NM_001304717.5:c.713_714delinsAC	NP_001291646.4:p.Tyr238=
NM_001304718.2:c.-541-5504_-541-5503delinsAC	NP_001291647.1:n.-541-5504_-541-5503delinsAC
NM_000314.8:c.194_195delinsAC MANE Select	NP_000305.3:p.Tyr65=