Canonical Allele Identifier: CA2695200942

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933037_87933081del , CM000672.2:g.87933037_87933081del	GRCh38
NC_000010.10:g.89692794_89692838del , CM000672.1:g.89692794_89692838del	GRCh37
NC_000010.9:g.89682774_89682818del	NCBI36
NG_007466.2:g.74599_74643del , LRG_311:g.74599_74643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.278_322del	ENSP00000514759.2:p.His93_Asp107del
ENST00000710265.1:c.278_322del	ENSP00000518161.1:p.His93_Asp107del
ENST00000472832.3:c.278_322del	ENSP00000483066.2:p.His93_Asp107del
ENST00000688158.2:n.1013_1057del
ENST00000688922.2:c.*108_*152del	ENSP00000508742.2:n.*108_*152del
ENST00000700021.1:c.233_277del	ENSP00000514757.1:p.His78_Asp92del
ENST00000700022.1:c.278_322del	ENSP00000514758.1:p.His93_Asp107del
ENST00000700029.1:c.112_156del
ENST00000706954.1:c.278_322del	ENSP00000516674.1:p.His93_Asp107del
ENST00000706955.1:c.*313_*357del	ENSP00000516675.1:n.*313_*357del
ENST00000686459.1:c.278_322del	ENSP00000508909.1:p.His93_Asp107del
ENST00000688158.1:c.*389_*433del	ENSP00000509254.1:n.*389_*433del
ENST00000688308.1:c.278_322del	ENSP00000508752.1:p.His93_Asp107del
ENST00000688922.1:c.199_243del
ENST00000693560.1:c.797_841del	ENSP00000509861.1:p.His266_Asp280del
ENST00000371953.8:c.278_322del MANE Select	ENSP00000361021.3:p.His93_Asp107del
ENST00000371953.7:c.278_322del	ENSP00000361021.3:p.His93_Asp107del
ENST00000498703.1:n.104_148del
ENST00000610634.1:c.176_220del	ENSP00000477517.1:p.His59_Asp73del
NM_000314.5:c.278_322del	NP_000305.3:p.His93_Asp107del
NM_000314.6:c.278_322del	NP_000305.3:p.His93_Asp107del
NM_001304717.2:c.797_841del	NP_001291646.2:p.His266_Asp280del
NM_001304718.1:c.-473_-429del	NP_001291647.1:n.-473_-429del
XM_006717926.2:c.233_277del	XP_006717989.1:p.His78_Asp92del
XM_011539981.1:c.278_322del	XP_011538283.1:p.His93_Asp107del
XM_011539982.1:c.182_226del	XP_011538284.1:p.His61_Asp75del
XR_945789.1:n.990_1034del
XR_945790.1:n.990_1034del
XR_945791.1:n.990_1034del
NM_000314.7:c.278_322del	NP_000305.3:p.His93_Asp107del
NM_001304717.5:c.797_841del	NP_001291646.4:p.His266_Asp280del
NM_001304718.2:c.-473_-429del	NP_001291647.1:n.-473_-429del
NM_000314.8:c.278_322del MANE Select	NP_000305.3:p.His93_Asp107del