Canonical Allele Identifier: CA2524984040

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965513_87965514del , CM000672.2:g.87965513_87965514del	GRCh38
NC_000010.10:g.89725270_89725271del , CM000672.1:g.89725270_89725271del	GRCh37
NC_000010.9:g.89715250_89715251del	NCBI36
NG_007466.2:g.107075_107076del , LRG_311:g.107075_107076del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*41_*42del	ENSP00000514759.2:n.*41_*42del
ENST00000710265.1:c.*282_*283del	ENSP00000518161.1:n.*282_*283del
ENST00000688158.2:n.1988_1989del
ENST00000688922.2:c.*1083_*1084del	ENSP00000508742.2:n.*1083_*1084del
ENST00000700021.1:c.*41_*42del	ENSP00000514757.1:n.*41_*42del
ENST00000700022.1:c.*592_*593del	ENSP00000514758.1:n.*592_*593del
ENST00000700023.1:n.2411_2412del
ENST00000700024.1:n.2645_2646del
ENST00000706954.1:c.*41_*42del	ENSP00000516674.1:n.*41_*42del
ENST00000706955.1:c.*1288_*1289del	ENSP00000516675.1:n.*1288_*1289del
ENST00000686459.1:c.*839_*840del	ENSP00000508909.1:n.*839_*840del
ENST00000688158.1:c.*1364_*1365del	ENSP00000509254.1:n.*1364_*1365del
ENST00000688308.1:c.*41_*42del	ENSP00000508752.1:n.*41_*42del
ENST00000688922.1:c.1174_1175del
ENST00000693560.1:c.*41_*42del	ENSP00000509861.1:n.*41_*42del
ENST00000371953.8:c.*41_*42del MANE Select	ENSP00000361021.3:n.*41_*42del
ENST00000371953.7:c.*41_*42del	ENSP00000361021.3:n.*41_*42del
NM_000314.5:c.*41_*42del	NP_000305.3:n.*41_*42del
NM_000314.6:c.*41_*42del	NP_000305.3:n.*41_*42del
NM_001304717.2:c.*41_*42del	NP_001291646.2:n.*41_*42del
NM_001304718.1:c.*41_*42del	NP_001291647.1:n.*41_*42del
XM_006717926.2:c.*41_*42del	XP_006717989.1:n.*41_*42del
XM_011539982.1:c.*41_*42del	XP_011538284.1:n.*41_*42del
XR_945791.1:n.1823_1824del
NM_000314.7:c.*41_*42del	NP_000305.3:n.*41_*42del
NM_001304717.5:c.*41_*42del	NP_001291646.4:n.*41_*42del
NM_001304718.2:c.*41_*42del	NP_001291647.1:n.*41_*42del
NM_000314.8:c.*41_*42del MANE Select	NP_000305.3:n.*41_*42del