Canonical Allele Identifier: CA2579926565

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965368_87965370del , CM000672.2:g.87965368_87965370del	GRCh38
NC_000010.10:g.89725125_89725127del , CM000672.1:g.89725125_89725127del	GRCh37
NC_000010.9:g.89715105_89715107del	NCBI36
NG_007466.2:g.106930_106932del , LRG_311:g.106930_106932del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1201_1203del	ENSP00000514759.2:p.Ser401del
ENST00000710265.1:c.*137_*139del	ENSP00000518161.1:n.*137_*139del
ENST00000688158.2:n.1843_1845del
ENST00000688922.2:c.*938_*940del	ENSP00000508742.2:n.*938_*940del
ENST00000700021.1:c.1063_1065del	ENSP00000514757.1:p.Ser355del
ENST00000700022.1:c.*447_*449del	ENSP00000514758.1:n.*447_*449del
ENST00000700023.1:n.2266_2268del
ENST00000700024.1:n.2500_2502del
ENST00000706954.1:c.1108_1110del	ENSP00000516674.1:p.Ser370del
ENST00000706955.1:c.*1143_*1145del	ENSP00000516675.1:n.*1143_*1145del
ENST00000686459.1:c.*694_*696del	ENSP00000508909.1:n.*694_*696del
ENST00000688158.1:c.*1219_*1221del	ENSP00000509254.1:n.*1219_*1221del
ENST00000688308.1:c.1108_1110del	ENSP00000508752.1:p.Ser370del
ENST00000688922.1:c.1029_1031del
ENST00000693560.1:c.1627_1629del	ENSP00000509861.1:p.Ser543del
ENST00000371953.8:c.1108_1110del MANE Select	ENSP00000361021.3:p.Ser370del
ENST00000371953.7:c.1108_1110del	ENSP00000361021.3:p.Ser370del
NM_000314.5:c.1108_1110del	NP_000305.3:p.Ser370del
NM_000314.6:c.1108_1110del	NP_000305.3:p.Ser370del
NM_001304717.2:c.1627_1629del	NP_001291646.2:p.Ser543del
NM_001304718.1:c.517_519del	NP_001291647.1:p.Ser173del
XM_006717926.2:c.1063_1065del	XP_006717989.1:p.Ser355del
XM_011539982.1:c.1012_1014del	XP_011538284.1:p.Ser338del
XR_945791.1:n.1678_1680del
NM_000314.7:c.1108_1110del	NP_000305.3:p.Ser370del
NM_001304717.5:c.1627_1629del	NP_001291646.4:p.Ser543del
NM_001304718.2:c.517_519del	NP_001291647.1:p.Ser173del
NM_000314.8:c.1108_1110del MANE Select	NP_000305.3:p.Ser370del