Canonical Allele Identifier: CA891836816

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961074_87961076delinsTAT , CM000672.2:g.87961074_87961076delinsTAT	GRCh38
NC_000010.10:g.89720831_89720833delinsTAT , CM000672.1:g.89720831_89720833delinsTAT	GRCh37
NC_000010.9:g.89710811_89710813delinsTAT	NCBI36
NG_007466.2:g.102636_102638delinsTAT , LRG_311:g.102636_102638delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1075_1077delinsTAT	ENSP00000514759.2:p.Ala359Tyr
ENST00000710265.1:c.982_984delinsTAT	ENSP00000518161.1:p.Ala328Tyr
ENST00000472832.3:c.982_984delinsTAT	ENSP00000483066.2:p.Ala328Tyr
ENST00000688158.2:n.1717_1719delinsTAT
ENST00000688922.2:c.*812_*814delinsTAT	ENSP00000508742.2:n.*812_*814delinsTAT
ENST00000700021.1:c.937_939delinsTAT	ENSP00000514757.1:p.Ala313Tyr
ENST00000700022.1:c.*321_*323delinsTAT	ENSP00000514758.1:n.*321_*323delinsTAT
ENST00000700023.1:n.2140_2142delinsTAT
ENST00000700024.1:n.2374_2376delinsTAT
ENST00000700025.1:n.1751_1753delinsTAT
ENST00000700026.1:n.619_621delinsTAT
ENST00000706954.1:c.982_984delinsTAT	ENSP00000516674.1:p.Ala328Tyr
ENST00000706955.1:c.*1017_*1019delinsTAT	ENSP00000516675.1:n.*1017_*1019delinsTAT
ENST00000686459.1:c.*568_*570delinsTAT	ENSP00000508909.1:n.*568_*570delinsTAT
ENST00000688158.1:c.*1093_*1095delinsTAT	ENSP00000509254.1:n.*1093_*1095delinsTAT
ENST00000688308.1:c.982_984delinsTAT	ENSP00000508752.1:p.Ala328Tyr
ENST00000688922.1:c.903_905delinsTAT
ENST00000693560.1:c.1501_1503delinsTAT	ENSP00000509861.1:p.Ala501Tyr
ENST00000371953.8:c.982_984delinsTAT MANE Select	ENSP00000361021.3:p.Ala328Tyr
ENST00000371953.7:c.982_984delinsTAT	ENSP00000361021.3:p.Ala328Tyr
ENST00000472832.2:c.409_411delinsTAT	ENSP00000483066.1:p.Ala137Tyr
NM_000314.5:c.982_984delinsTAT	NP_000305.3:p.Ala328Tyr
NM_000314.6:c.982_984delinsTAT	NP_000305.3:p.Ala328Tyr
NM_001304717.2:c.1501_1503delinsTAT	NP_001291646.2:p.Ala501Tyr
NM_001304718.1:c.391_393delinsTAT	NP_001291647.1:p.Ala131Tyr
XM_006717926.2:c.937_939delinsTAT	XP_006717989.1:p.Ala313Tyr
XM_011539981.1:c.982_984delinsTAT	XP_011538283.1:p.Ala328Tyr
XM_011539982.1:c.886_888delinsTAT	XP_011538284.1:p.Ala296Tyr
XR_945791.1:n.1552_1554delinsTAT
NM_000314.7:c.982_984delinsTAT	NP_000305.3:p.Ala328Tyr
NM_001304717.5:c.1501_1503delinsTAT	NP_001291646.4:p.Ala501Tyr
NM_001304718.2:c.391_393delinsTAT	NP_001291647.1:p.Ala131Tyr
NM_000314.8:c.982_984delinsTAT MANE Select	NP_000305.3:p.Ala328Tyr