Canonical Allele Identifier: CA2579926419

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965380_87965382del , CM000672.2:g.87965380_87965382del	GRCh38
NC_000010.10:g.89725137_89725139del , CM000672.1:g.89725137_89725139del	GRCh37
NC_000010.9:g.89715117_89715119del	NCBI36
NG_007466.2:g.106942_106944del , LRG_311:g.106942_106944del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1213_1215del	ENSP00000514759.2:p.Pro405del
ENST00000710265.1:c.*149_*151del	ENSP00000518161.1:n.*149_*151del
ENST00000688158.2:n.1855_1857del
ENST00000688922.2:c.*950_*952del	ENSP00000508742.2:n.*950_*952del
ENST00000700021.1:c.1075_1077del	ENSP00000514757.1:p.Pro359del
ENST00000700022.1:c.*459_*461del	ENSP00000514758.1:n.*459_*461del
ENST00000700023.1:n.2278_2280del
ENST00000700024.1:n.2512_2514del
ENST00000706954.1:c.1120_1122del	ENSP00000516674.1:p.Pro374del
ENST00000706955.1:c.*1155_*1157del	ENSP00000516675.1:n.*1155_*1157del
ENST00000686459.1:c.*706_*708del	ENSP00000508909.1:n.*706_*708del
ENST00000688158.1:c.*1231_*1233del	ENSP00000509254.1:n.*1231_*1233del
ENST00000688308.1:c.1120_1122del	ENSP00000508752.1:p.Pro374del
ENST00000688922.1:c.1041_1043del
ENST00000693560.1:c.1639_1641del	ENSP00000509861.1:p.Pro547del
ENST00000371953.8:c.1120_1122del MANE Select	ENSP00000361021.3:p.Pro374del
ENST00000371953.7:c.1120_1122del	ENSP00000361021.3:p.Pro374del
NM_000314.5:c.1120_1122del	NP_000305.3:p.Pro374del
NM_000314.6:c.1120_1122del	NP_000305.3:p.Pro374del
NM_001304717.2:c.1639_1641del	NP_001291646.2:p.Pro547del
NM_001304718.1:c.529_531del	NP_001291647.1:p.Pro177del
XM_006717926.2:c.1075_1077del	XP_006717989.1:p.Pro359del
XM_011539982.1:c.1024_1026del	XP_011538284.1:p.Pro342del
XR_945791.1:n.1690_1692del
NM_000314.7:c.1120_1122del	NP_000305.3:p.Pro374del
NM_001304717.5:c.1639_1641del	NP_001291646.4:p.Pro547del
NM_001304718.2:c.529_531del	NP_001291647.1:p.Pro177del
NM_000314.8:c.1120_1122del MANE Select	NP_000305.3:p.Pro374del