Canonical Allele Identifier: CA891840187

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960900_87960902delinsGTT , CM000672.2:g.87960900_87960902delinsGTT	GRCh38
NC_000010.10:g.89720657_89720659delinsGTT , CM000672.1:g.89720657_89720659delinsGTT	GRCh37
NC_000010.9:g.89710637_89710639delinsGTT	NCBI36
NG_007466.2:g.102462_102464delinsGTT , LRG_311:g.102462_102464delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.901_903delinsGTT	ENSP00000514759.2:p.Met301Val
ENST00000710265.1:c.808_810delinsGTT	ENSP00000518161.1:p.Met270Val
ENST00000472832.3:c.808_810delinsGTT	ENSP00000483066.2:p.Met270Val
ENST00000688158.2:n.1543_1545delinsGTT
ENST00000688922.2:c.*638_*640delinsGTT	ENSP00000508742.2:n.*638_*640delinsGTT
ENST00000700021.1:c.763_765delinsGTT	ENSP00000514757.1:p.Met255Val
ENST00000700022.1:c.*147_*149delinsGTT	ENSP00000514758.1:n.*147_*149delinsGTT
ENST00000700023.1:n.1966_1968delinsGTT
ENST00000700024.1:n.2200_2202delinsGTT
ENST00000700025.1:n.1577_1579delinsGTT
ENST00000700026.1:n.445_447delinsGTT
ENST00000700029.1:c.735_737delinsGTT
ENST00000706954.1:c.808_810delinsGTT	ENSP00000516674.1:p.Met270Val
ENST00000706955.1:c.*843_*845delinsGTT	ENSP00000516675.1:n.*843_*845delinsGTT
ENST00000686459.1:c.*394_*396delinsGTT	ENSP00000508909.1:n.*394_*396delinsGTT
ENST00000688158.1:c.*919_*921delinsGTT	ENSP00000509254.1:n.*919_*921delinsGTT
ENST00000688308.1:c.808_810delinsGTT	ENSP00000508752.1:p.Met270Val
ENST00000688922.1:c.729_731delinsGTT
ENST00000693560.1:c.1327_1329delinsGTT	ENSP00000509861.1:p.Met443Val
ENST00000371953.8:c.808_810delinsGTT MANE Select	ENSP00000361021.3:p.Met270Val
ENST00000371953.7:c.808_810delinsGTT	ENSP00000361021.3:p.Met270Val
ENST00000472832.2:c.235_237delinsGTT	ENSP00000483066.1:p.Met79Val
NM_000314.5:c.808_810delinsGTT	NP_000305.3:p.Met270Val
NM_000314.6:c.808_810delinsGTT	NP_000305.3:p.Met270Val
NM_001304717.2:c.1327_1329delinsGTT	NP_001291646.2:p.Met443Val
NM_001304718.1:c.217_219delinsGTT	NP_001291647.1:p.Met73Val
XM_006717926.2:c.763_765delinsGTT	XP_006717989.1:p.Met255Val
XM_011539981.1:c.808_810delinsGTT	XP_011538283.1:p.Met270Val
XM_011539982.1:c.712_714delinsGTT	XP_011538284.1:p.Met238Val
XR_945791.1:n.1378_1380delinsGTT
NM_000314.7:c.808_810delinsGTT	NP_000305.3:p.Met270Val
NM_001304717.5:c.1327_1329delinsGTT	NP_001291646.4:p.Met443Val
NM_001304718.2:c.217_219delinsGTT	NP_001291647.1:p.Met73Val
NM_000314.8:c.808_810delinsGTT MANE Select	NP_000305.3:p.Met270Val