Canonical Allele Identifier: CA891834863

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925529_87925531delinsTGG , CM000672.2:g.87925529_87925531delinsTGG	GRCh38
NC_000010.10:g.89685286_89685288delinsTGG , CM000672.1:g.89685286_89685288delinsTGG	GRCh37
NC_000010.9:g.89675266_89675268delinsTGG	NCBI36
NG_007466.2:g.67091_67093delinsTGG , LRG_311:g.67091_67093delinsTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.181_183delinsTGG	ENSP00000514759.2:p.His61Trp
ENST00000710265.1:c.181_183delinsTGG	ENSP00000518161.1:p.His61Trp
ENST00000472832.3:c.181_183delinsTGG	ENSP00000483066.2:p.His61Trp
ENST00000688158.2:n.916_918delinsTGG
ENST00000688922.2:c.181_183delinsTGG	ENSP00000508742.2:p.His61Trp
ENST00000700021.1:c.165-5517_165-5515delinsTGG	ENSP00000514757.1:n.165-5517_165-5515deli...
ENST00000700022.1:c.181_183delinsTGG	ENSP00000514758.1:p.His61Trp
ENST00000700029.1:c.15_17delinsTGG
ENST00000706954.1:c.181_183delinsTGG	ENSP00000516674.1:p.His61Trp
ENST00000706955.1:c.*216_*218delinsTGG	ENSP00000516675.1:n.*216_*218delinsTGG
ENST00000686459.1:c.181_183delinsTGG	ENSP00000508909.1:p.His61Trp
ENST00000688158.1:c.*292_*294delinsTGG	ENSP00000509254.1:n.*292_*294delinsTGG
ENST00000688308.1:c.181_183delinsTGG	ENSP00000508752.1:p.His61Trp
ENST00000688922.1:c.50_52delinsTGG
ENST00000693560.1:c.700_702delinsTGG	ENSP00000509861.1:p.His234Trp
ENST00000371953.8:c.181_183delinsTGG MANE Select	ENSP00000361021.3:p.His61Trp
ENST00000371953.7:c.181_183delinsTGG	ENSP00000361021.3:p.His61Trp
ENST00000498703.1:n.7_9delinsTGG
ENST00000610634.1:c.79_81delinsTGG	ENSP00000477517.1:p.His27Trp
NM_000314.5:c.181_183delinsTGG	NP_000305.3:p.His61Trp
NM_000314.6:c.181_183delinsTGG	NP_000305.3:p.His61Trp
NM_001304717.2:c.700_702delinsTGG	NP_001291646.2:p.His234Trp
NM_001304718.1:c.-541-5517_-541-5515delinsTGG	NP_001291647.1:n.-541-5517_-541-5515delin...
XM_006717926.2:c.165-5517_165-5515delinsTGG	XP_006717989.1:n.165-5517_165-5515delinsT...
XM_011539981.1:c.181_183delinsTGG	XP_011538283.1:p.His61Trp
XM_011539982.1:c.85_87delinsTGG	XP_011538284.1:p.His29Trp
XR_945789.1:n.893_895delinsTGG
XR_945790.1:n.893_895delinsTGG
XR_945791.1:n.893_895delinsTGG
NM_000314.7:c.181_183delinsTGG	NP_000305.3:p.His61Trp
NM_001304717.5:c.700_702delinsTGG	NP_001291646.4:p.His234Trp
NM_001304718.2:c.-541-5517_-541-5515delinsTGG	NP_001291647.1:n.-541-5517_-541-5515delin...
NM_000314.8:c.181_183delinsTGG MANE Select	NP_000305.3:p.His61Trp