Canonical Allele Identifier: CA891835069

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925542_87925543delinsGG , CM000672.2:g.87925542_87925543delinsGG	GRCh38
NC_000010.10:g.89685299_89685300delinsGG , CM000672.1:g.89685299_89685300delinsGG	GRCh37
NC_000010.9:g.89675279_89675280delinsGG	NCBI36
NG_007466.2:g.67104_67105delinsGG , LRG_311:g.67104_67105delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.194_195delinsGG	ENSP00000514759.2:p.Tyr65Trp
ENST00000710265.1:c.194_195delinsGG	ENSP00000518161.1:p.Tyr65Trp
ENST00000472832.3:c.194_195delinsGG	ENSP00000483066.2:p.Tyr65Trp
ENST00000688158.2:n.929_930delinsGG
ENST00000688922.2:c.194_195delinsGG	ENSP00000508742.2:p.Tyr65Trp
ENST00000700021.1:c.165-5504_165-5503delinsGG	ENSP00000514757.1:n.165-5504_165-5503delinsGG
ENST00000700022.1:c.194_195delinsGG	ENSP00000514758.1:p.Tyr65Trp
ENST00000700029.1:c.28_29delinsGG
ENST00000706954.1:c.194_195delinsGG	ENSP00000516674.1:p.Tyr65Trp
ENST00000706955.1:c.*229_*230delinsGG	ENSP00000516675.1:n.*229_*230delinsGG
ENST00000686459.1:c.194_195delinsGG	ENSP00000508909.1:p.Tyr65Trp
ENST00000688158.1:c.*305_*306delinsGG	ENSP00000509254.1:n.*305_*306delinsGG
ENST00000688308.1:c.194_195delinsGG	ENSP00000508752.1:p.Tyr65Trp
ENST00000688922.1:c.63_64delinsGG
ENST00000693560.1:c.713_714delinsGG	ENSP00000509861.1:p.Tyr238Trp
ENST00000371953.8:c.194_195delinsGG MANE Select	ENSP00000361021.3:p.Tyr65Trp
ENST00000371953.7:c.194_195delinsGG	ENSP00000361021.3:p.Tyr65Trp
ENST00000498703.1:n.20_21delinsGG
ENST00000610634.1:c.92_93delinsGG	ENSP00000477517.1:p.Tyr31Trp
NM_000314.5:c.194_195delinsGG	NP_000305.3:p.Tyr65Trp
NM_000314.6:c.194_195delinsGG	NP_000305.3:p.Tyr65Trp
NM_001304717.2:c.713_714delinsGG	NP_001291646.2:p.Tyr238Trp
NM_001304718.1:c.-541-5504_-541-5503delinsGG	NP_001291647.1:n.-541-5504_-541-5503delinsGG
XM_006717926.2:c.165-5504_165-5503delinsGG	XP_006717989.1:n.165-5504_165-5503delinsGG
XM_011539981.1:c.194_195delinsGG	XP_011538283.1:p.Tyr65Trp
XM_011539982.1:c.98_99delinsGG	XP_011538284.1:p.Tyr33Trp
XR_945789.1:n.906_907delinsGG
XR_945790.1:n.906_907delinsGG
XR_945791.1:n.906_907delinsGG
NM_000314.7:c.194_195delinsGG	NP_000305.3:p.Tyr65Trp
NM_001304717.5:c.713_714delinsGG	NP_001291646.4:p.Tyr238Trp
NM_001304718.2:c.-541-5504_-541-5503delinsGG	NP_001291647.1:n.-541-5504_-541-5503delinsGG
NM_000314.8:c.194_195delinsGG MANE Select	NP_000305.3:p.Tyr65Trp