Canonical Allele Identifier: CA891840190

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960901_87960902delinsGA , CM000672.2:g.87960901_87960902delinsGA	GRCh38
NC_000010.10:g.89720658_89720659delinsGA , CM000672.1:g.89720658_89720659delinsGA	GRCh37
NC_000010.9:g.89710638_89710639delinsGA	NCBI36
NG_007466.2:g.102463_102464delinsGA , LRG_311:g.102463_102464delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.902_903delinsGA	ENSP00000514759.2:p.Met301Arg
ENST00000710265.1:c.809_810delinsGA	ENSP00000518161.1:p.Met270Arg
ENST00000472832.3:c.809_810delinsGA	ENSP00000483066.2:p.Met270Arg
ENST00000688158.2:n.1544_1545delinsGA
ENST00000688922.2:c.*639_*640delinsGA	ENSP00000508742.2:n.*639_*640delinsGA
ENST00000700021.1:c.764_765delinsGA	ENSP00000514757.1:p.Met255Arg
ENST00000700022.1:c.*148_*149delinsGA	ENSP00000514758.1:n.*148_*149delinsGA
ENST00000700023.1:n.1967_1968delinsGA
ENST00000700024.1:n.2201_2202delinsGA
ENST00000700025.1:n.1578_1579delinsGA
ENST00000700026.1:n.446_447delinsGA
ENST00000700029.1:c.736_737delinsGA
ENST00000706954.1:c.809_810delinsGA	ENSP00000516674.1:p.Met270Arg
ENST00000706955.1:c.*844_*845delinsGA	ENSP00000516675.1:n.*844_*845delinsGA
ENST00000686459.1:c.*395_*396delinsGA	ENSP00000508909.1:n.*395_*396delinsGA
ENST00000688158.1:c.*920_*921delinsGA	ENSP00000509254.1:n.*920_*921delinsGA
ENST00000688308.1:c.809_810delinsGA	ENSP00000508752.1:p.Met270Arg
ENST00000688922.1:c.730_731delinsGA
ENST00000693560.1:c.1328_1329delinsGA	ENSP00000509861.1:p.Met443Arg
ENST00000371953.8:c.809_810delinsGA MANE Select	ENSP00000361021.3:p.Met270Arg
ENST00000371953.7:c.809_810delinsGA	ENSP00000361021.3:p.Met270Arg
ENST00000472832.2:c.236_237delinsGA	ENSP00000483066.1:p.Met79Arg
NM_000314.5:c.809_810delinsGA	NP_000305.3:p.Met270Arg
NM_000314.6:c.809_810delinsGA	NP_000305.3:p.Met270Arg
NM_001304717.2:c.1328_1329delinsGA	NP_001291646.2:p.Met443Arg
NM_001304718.1:c.218_219delinsGA	NP_001291647.1:p.Met73Arg
XM_006717926.2:c.764_765delinsGA	XP_006717989.1:p.Met255Arg
XM_011539981.1:c.809_810delinsGA	XP_011538283.1:p.Met270Arg
XM_011539982.1:c.713_714delinsGA	XP_011538284.1:p.Met238Arg
XR_945791.1:n.1379_1380delinsGA
NM_000314.7:c.809_810delinsGA	NP_000305.3:p.Met270Arg
NM_001304717.5:c.1328_1329delinsGA	NP_001291646.4:p.Met443Arg
NM_001304718.2:c.218_219delinsGA	NP_001291647.1:p.Met73Arg
NM_000314.8:c.809_810delinsGA MANE Select	NP_000305.3:p.Met270Arg