Canonical Allele Identifier: CA891836777

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961071_87961073delinsGAT , CM000672.2:g.87961071_87961073delinsGAT	GRCh38
NC_000010.10:g.89720828_89720830delinsGAT , CM000672.1:g.89720828_89720830delinsGAT	GRCh37
NC_000010.9:g.89710808_89710810delinsGAT	NCBI36
NG_007466.2:g.102633_102635delinsGAT , LRG_311:g.102633_102635delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1072_1074delinsGAT	ENSP00000514759.2:p.Lys358Asp
ENST00000710265.1:c.979_981delinsGAT	ENSP00000518161.1:p.Lys327Asp
ENST00000472832.3:c.979_981delinsGAT	ENSP00000483066.2:p.Lys327Asp
ENST00000688158.2:n.1714_1716delinsGAT
ENST00000688922.2:c.*809_*811delinsGAT	ENSP00000508742.2:n.*809_*811delinsGAT
ENST00000700021.1:c.934_936delinsGAT	ENSP00000514757.1:p.Lys312Asp
ENST00000700022.1:c.*318_*320delinsGAT	ENSP00000514758.1:n.*318_*320delinsGAT
ENST00000700023.1:n.2137_2139delinsGAT
ENST00000700024.1:n.2371_2373delinsGAT
ENST00000700025.1:n.1748_1750delinsGAT
ENST00000700026.1:n.616_618delinsGAT
ENST00000706954.1:c.979_981delinsGAT	ENSP00000516674.1:p.Lys327Asp
ENST00000706955.1:c.*1014_*1016delinsGAT	ENSP00000516675.1:n.*1014_*1016delinsGAT
ENST00000686459.1:c.*565_*567delinsGAT	ENSP00000508909.1:n.*565_*567delinsGAT
ENST00000688158.1:c.*1090_*1092delinsGAT	ENSP00000509254.1:n.*1090_*1092delinsGAT
ENST00000688308.1:c.979_981delinsGAT	ENSP00000508752.1:p.Lys327Asp
ENST00000688922.1:c.900_902delinsGAT
ENST00000693560.1:c.1498_1500delinsGAT	ENSP00000509861.1:p.Lys500Asp
ENST00000371953.8:c.979_981delinsGAT MANE Select	ENSP00000361021.3:p.Lys327Asp
ENST00000371953.7:c.979_981delinsGAT	ENSP00000361021.3:p.Lys327Asp
ENST00000472832.2:c.406_408delinsGAT	ENSP00000483066.1:p.Lys136Asp
NM_000314.5:c.979_981delinsGAT	NP_000305.3:p.Lys327Asp
NM_000314.6:c.979_981delinsGAT	NP_000305.3:p.Lys327Asp
NM_001304717.2:c.1498_1500delinsGAT	NP_001291646.2:p.Lys500Asp
NM_001304718.1:c.388_390delinsGAT	NP_001291647.1:p.Lys130Asp
XM_006717926.2:c.934_936delinsGAT	XP_006717989.1:p.Lys312Asp
XM_011539981.1:c.979_981delinsGAT	XP_011538283.1:p.Lys327Asp
XM_011539982.1:c.883_885delinsGAT	XP_011538284.1:p.Lys295Asp
XR_945791.1:n.1549_1551delinsGAT
NM_000314.7:c.979_981delinsGAT	NP_000305.3:p.Lys327Asp
NM_001304717.5:c.1498_1500delinsGAT	NP_001291646.4:p.Lys500Asp
NM_001304718.2:c.388_390delinsGAT	NP_001291647.1:p.Lys130Asp
NM_000314.8:c.979_981delinsGAT MANE Select	NP_000305.3:p.Lys327Asp