Canonical Allele Identifier: CA891836822

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961075_87961076delinsGT , CM000672.2:g.87961075_87961076delinsGT	GRCh38
NC_000010.10:g.89720832_89720833delinsGT , CM000672.1:g.89720832_89720833delinsGT	GRCh37
NC_000010.9:g.89710812_89710813delinsGT	NCBI36
NG_007466.2:g.102637_102638delinsGT , LRG_311:g.102637_102638delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1076_1077delinsGT	ENSP00000514759.2:p.Ala359Gly
ENST00000710265.1:c.983_984delinsGT	ENSP00000518161.1:p.Ala328Gly
ENST00000472832.3:c.983_984delinsGT	ENSP00000483066.2:p.Ala328Gly
ENST00000688158.2:n.1718_1719delinsGT
ENST00000688922.2:c.*813_*814delinsGT	ENSP00000508742.2:n.*813_*814delinsGT
ENST00000700021.1:c.938_939delinsGT	ENSP00000514757.1:p.Ala313Gly
ENST00000700022.1:c.*322_*323delinsGT	ENSP00000514758.1:n.*322_*323delinsGT
ENST00000700023.1:n.2141_2142delinsGT
ENST00000700024.1:n.2375_2376delinsGT
ENST00000700025.1:n.1752_1753delinsGT
ENST00000700026.1:n.620_621delinsGT
ENST00000706954.1:c.983_984delinsGT	ENSP00000516674.1:p.Ala328Gly
ENST00000706955.1:c.*1018_*1019delinsGT	ENSP00000516675.1:n.*1018_*1019delinsGT
ENST00000686459.1:c.*569_*570delinsGT	ENSP00000508909.1:n.*569_*570delinsGT
ENST00000688158.1:c.*1094_*1095delinsGT	ENSP00000509254.1:n.*1094_*1095delinsGT
ENST00000688308.1:c.983_984delinsGT	ENSP00000508752.1:p.Ala328Gly
ENST00000688922.1:c.904_905delinsGT
ENST00000693560.1:c.1502_1503delinsGT	ENSP00000509861.1:p.Ala501Gly
ENST00000371953.8:c.983_984delinsGT MANE Select	ENSP00000361021.3:p.Ala328Gly
ENST00000371953.7:c.983_984delinsGT	ENSP00000361021.3:p.Ala328Gly
ENST00000472832.2:c.410_411delinsGT	ENSP00000483066.1:p.Ala137Gly
NM_000314.5:c.983_984delinsGT	NP_000305.3:p.Ala328Gly
NM_000314.6:c.983_984delinsGT	NP_000305.3:p.Ala328Gly
NM_001304717.2:c.1502_1503delinsGT	NP_001291646.2:p.Ala501Gly
NM_001304718.1:c.392_393delinsGT	NP_001291647.1:p.Ala131Gly
XM_006717926.2:c.938_939delinsGT	XP_006717989.1:p.Ala313Gly
XM_011539981.1:c.983_984delinsGT	XP_011538283.1:p.Ala328Gly
XM_011539982.1:c.887_888delinsGT	XP_011538284.1:p.Ala296Gly
XR_945791.1:n.1553_1554delinsGT
NM_000314.7:c.983_984delinsGT	NP_000305.3:p.Ala328Gly
NM_001304717.5:c.1502_1503delinsGT	NP_001291646.4:p.Ala501Gly
NM_001304718.2:c.392_393delinsGT	NP_001291647.1:p.Ala131Gly
NM_000314.8:c.983_984delinsGT MANE Select	NP_000305.3:p.Ala328Gly