Canonical Allele Identifier: CA891840191

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960901_87960902delinsAT , CM000672.2:g.87960901_87960902delinsAT	GRCh38
NC_000010.10:g.89720658_89720659delinsAT , CM000672.1:g.89720658_89720659delinsAT	GRCh37
NC_000010.9:g.89710638_89710639delinsAT	NCBI36
NG_007466.2:g.102463_102464delinsAT , LRG_311:g.102463_102464delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.902_903delinsAT	ENSP00000514759.2:p.Met301Asn
ENST00000710265.1:c.809_810delinsAT	ENSP00000518161.1:p.Met270Asn
ENST00000472832.3:c.809_810delinsAT	ENSP00000483066.2:p.Met270Asn
ENST00000688158.2:n.1544_1545delinsAT
ENST00000688922.2:c.*639_*640delinsAT	ENSP00000508742.2:n.*639_*640delinsAT
ENST00000700021.1:c.764_765delinsAT	ENSP00000514757.1:p.Met255Asn
ENST00000700022.1:c.*148_*149delinsAT	ENSP00000514758.1:n.*148_*149delinsAT
ENST00000700023.1:n.1967_1968delinsAT
ENST00000700024.1:n.2201_2202delinsAT
ENST00000700025.1:n.1578_1579delinsAT
ENST00000700026.1:n.446_447delinsAT
ENST00000700029.1:c.736_737delinsAT
ENST00000706954.1:c.809_810delinsAT	ENSP00000516674.1:p.Met270Asn
ENST00000706955.1:c.*844_*845delinsAT	ENSP00000516675.1:n.*844_*845delinsAT
ENST00000686459.1:c.*395_*396delinsAT	ENSP00000508909.1:n.*395_*396delinsAT
ENST00000688158.1:c.*920_*921delinsAT	ENSP00000509254.1:n.*920_*921delinsAT
ENST00000688308.1:c.809_810delinsAT	ENSP00000508752.1:p.Met270Asn
ENST00000688922.1:c.730_731delinsAT
ENST00000693560.1:c.1328_1329delinsAT	ENSP00000509861.1:p.Met443Asn
ENST00000371953.8:c.809_810delinsAT MANE Select	ENSP00000361021.3:p.Met270Asn
ENST00000371953.7:c.809_810delinsAT	ENSP00000361021.3:p.Met270Asn
ENST00000472832.2:c.236_237delinsAT	ENSP00000483066.1:p.Met79Asn
NM_000314.5:c.809_810delinsAT	NP_000305.3:p.Met270Asn
NM_000314.6:c.809_810delinsAT	NP_000305.3:p.Met270Asn
NM_001304717.2:c.1328_1329delinsAT	NP_001291646.2:p.Met443Asn
NM_001304718.1:c.218_219delinsAT	NP_001291647.1:p.Met73Asn
XM_006717926.2:c.764_765delinsAT	XP_006717989.1:p.Met255Asn
XM_011539981.1:c.809_810delinsAT	XP_011538283.1:p.Met270Asn
XM_011539982.1:c.713_714delinsAT	XP_011538284.1:p.Met238Asn
XR_945791.1:n.1379_1380delinsAT
NM_000314.7:c.809_810delinsAT	NP_000305.3:p.Met270Asn
NM_001304717.5:c.1328_1329delinsAT	NP_001291646.4:p.Met443Asn
NM_001304718.2:c.218_219delinsAT	NP_001291647.1:p.Met73Asn
NM_000314.8:c.809_810delinsAT MANE Select	NP_000305.3:p.Met270Asn