Canonical Allele Identifier: CA891836209

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961020_87961022delinsTGG , CM000672.2:g.87961020_87961022delinsTGG	GRCh38
NC_000010.10:g.89720777_89720779delinsTGG , CM000672.1:g.89720777_89720779delinsTGG	GRCh37
NC_000010.9:g.89710757_89710759delinsTGG	NCBI36
NG_007466.2:g.102582_102584delinsTGG , LRG_311:g.102582_102584delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1021_1023delinsTGG	ENSP00000514759.2:p.Asp341Trp
ENST00000710265.1:c.928_930delinsTGG	ENSP00000518161.1:p.Asp310Trp
ENST00000472832.3:c.928_930delinsTGG	ENSP00000483066.2:p.Asp310Trp
ENST00000688158.2:n.1663_1665delinsTGG
ENST00000688922.2:c.*758_*760delinsTGG	ENSP00000508742.2:n.*758_*760delinsTGG
ENST00000700021.1:c.883_885delinsTGG	ENSP00000514757.1:p.Asp295Trp
ENST00000700022.1:c.*267_*269delinsTGG	ENSP00000514758.1:n.*267_*269delinsTGG
ENST00000700023.1:n.2086_2088delinsTGG
ENST00000700024.1:n.2320_2322delinsTGG
ENST00000700025.1:n.1697_1699delinsTGG
ENST00000700026.1:n.565_567delinsTGG
ENST00000706954.1:c.928_930delinsTGG	ENSP00000516674.1:p.Asp310Trp
ENST00000706955.1:c.*963_*965delinsTGG	ENSP00000516675.1:n.*963_*965delinsTGG
ENST00000686459.1:c.*514_*516delinsTGG	ENSP00000508909.1:n.*514_*516delinsTGG
ENST00000688158.1:c.*1039_*1041delinsTGG	ENSP00000509254.1:n.*1039_*1041delinsTGG
ENST00000688308.1:c.928_930delinsTGG	ENSP00000508752.1:p.Asp310Trp
ENST00000688922.1:c.849_851delinsTGG
ENST00000693560.1:c.1447_1449delinsTGG	ENSP00000509861.1:p.Asp483Trp
ENST00000371953.8:c.928_930delinsTGG MANE Select	ENSP00000361021.3:p.Asp310Trp
ENST00000371953.7:c.928_930delinsTGG	ENSP00000361021.3:p.Asp310Trp
ENST00000472832.2:c.355_357delinsTGG	ENSP00000483066.1:p.Asp119Trp
NM_000314.5:c.928_930delinsTGG	NP_000305.3:p.Asp310Trp
NM_000314.6:c.928_930delinsTGG	NP_000305.3:p.Asp310Trp
NM_001304717.2:c.1447_1449delinsTGG	NP_001291646.2:p.Asp483Trp
NM_001304718.1:c.337_339delinsTGG	NP_001291647.1:p.Asp113Trp
XM_006717926.2:c.883_885delinsTGG	XP_006717989.1:p.Asp295Trp
XM_011539981.1:c.928_930delinsTGG	XP_011538283.1:p.Asp310Trp
XM_011539982.1:c.832_834delinsTGG	XP_011538284.1:p.Asp278Trp
XR_945791.1:n.1498_1500delinsTGG
NM_000314.7:c.928_930delinsTGG	NP_000305.3:p.Asp310Trp
NM_001304717.5:c.1447_1449delinsTGG	NP_001291646.4:p.Asp483Trp
NM_001304718.2:c.337_339delinsTGG	NP_001291647.1:p.Asp113Trp
NM_000314.8:c.928_930delinsTGG MANE Select	NP_000305.3:p.Asp310Trp