Canonical Allele Identifier: CA891839384

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957871_87957872delinsAT , CM000672.2:g.87957871_87957872delinsAT	GRCh38
NC_000010.10:g.89717628_89717629delinsAT , CM000672.1:g.89717628_89717629delinsAT	GRCh37
NC_000010.9:g.89707608_89707609delinsAT	NCBI36
NG_007466.2:g.99433_99434delinsAT , LRG_311:g.99433_99434delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.653_654delinsAT	ENSP00000514759.2:p.Cys218Tyr
ENST00000710265.1:c.653_654delinsAT	ENSP00000518161.1:p.Cys218Tyr
ENST00000472832.3:c.653_654delinsAT	ENSP00000483066.2:p.Cys218Tyr
ENST00000688158.2:n.1388_1389delinsAT
ENST00000688922.2:c.*483_*484delinsAT	ENSP00000508742.2:n.*483_*484delinsAT
ENST00000700021.1:c.608_609delinsAT	ENSP00000514757.1:p.Cys203Tyr
ENST00000700022.1:c.511_512delinsAT	ENSP00000514758.1:p.Ala171Ile
ENST00000700023.1:n.1811_1812delinsAT
ENST00000700024.1:n.2045_2046delinsAT
ENST00000700025.1:n.1422_1423delinsAT
ENST00000700026.1:n.290_291delinsAT
ENST00000700029.1:c.487_488delinsAT
ENST00000706954.1:c.653_654delinsAT	ENSP00000516674.1:p.Cys218Tyr
ENST00000706955.1:c.*688_*689delinsAT	ENSP00000516675.1:n.*688_*689delinsAT
ENST00000686459.1:c.*239_*240delinsAT	ENSP00000508909.1:n.*239_*240delinsAT
ENST00000688158.1:c.*764_*765delinsAT	ENSP00000509254.1:n.*764_*765delinsAT
ENST00000688308.1:c.653_654delinsAT	ENSP00000508752.1:p.Cys218Tyr
ENST00000688922.1:c.574_575delinsAT
ENST00000693560.1:c.1172_1173delinsAT	ENSP00000509861.1:p.Cys391Tyr
ENST00000371953.8:c.653_654delinsAT MANE Select	ENSP00000361021.3:p.Cys218Tyr
ENST00000371953.7:c.653_654delinsAT	ENSP00000361021.3:p.Cys218Tyr
ENST00000472832.2:c.80_81delinsAT	ENSP00000483066.1:p.Cys27Tyr
NM_000314.5:c.653_654delinsAT	NP_000305.3:p.Cys218Tyr
NM_000314.6:c.653_654delinsAT	NP_000305.3:p.Cys218Tyr
NM_001304717.2:c.1172_1173delinsAT	NP_001291646.2:p.Cys391Tyr
NM_001304718.1:c.62_63delinsAT	NP_001291647.1:p.Cys21Tyr
XM_006717926.2:c.608_609delinsAT	XP_006717989.1:p.Cys203Tyr
XM_011539981.1:c.653_654delinsAT	XP_011538283.1:p.Cys218Tyr
XM_011539982.1:c.557_558delinsAT	XP_011538284.1:p.Cys186Tyr
XR_945791.1:n.1223_1224delinsAT
NM_000314.7:c.653_654delinsAT	NP_000305.3:p.Cys218Tyr
NM_001304717.5:c.1172_1173delinsAT	NP_001291646.4:p.Cys391Tyr
NM_001304718.2:c.62_63delinsAT	NP_001291647.1:p.Cys21Tyr
NM_000314.8:c.653_654delinsAT MANE Select	NP_000305.3:p.Cys218Tyr