Canonical Allele Identifier: CA2579926793

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960910_87960912del , CM000672.2:g.87960910_87960912del	GRCh38
NC_000010.10:g.89720667_89720669del , CM000672.1:g.89720667_89720669del	GRCh37
NC_000010.9:g.89710647_89710649del	NCBI36
NG_007466.2:g.102472_102474del , LRG_311:g.102472_102474del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.911_913del	ENSP00000514759.2:p.Phe304del
ENST00000710265.1:c.818_820del	ENSP00000518161.1:p.Phe273del
ENST00000472832.3:c.818_820del	ENSP00000483066.2:p.Phe273del
ENST00000688158.2:n.1553_1555del
ENST00000688922.2:c.*648_*650del	ENSP00000508742.2:n.*648_*650del
ENST00000700021.1:c.773_775del	ENSP00000514757.1:p.Phe258del
ENST00000700022.1:c.*157_*159del	ENSP00000514758.1:n.*157_*159del
ENST00000700023.1:n.1976_1978del
ENST00000700024.1:n.2210_2212del
ENST00000700025.1:n.1587_1589del
ENST00000700026.1:n.455_457del
ENST00000700029.1:c.745_747del
ENST00000706954.1:c.818_820del	ENSP00000516674.1:p.Phe273del
ENST00000706955.1:c.*853_*855del	ENSP00000516675.1:n.*853_*855del
ENST00000686459.1:c.*404_*406del	ENSP00000508909.1:n.*404_*406del
ENST00000688158.1:c.*929_*931del	ENSP00000509254.1:n.*929_*931del
ENST00000688308.1:c.818_820del	ENSP00000508752.1:p.Phe273del
ENST00000688922.1:c.739_741del
ENST00000693560.1:c.1337_1339del	ENSP00000509861.1:p.Phe446del
ENST00000371953.8:c.818_820del MANE Select	ENSP00000361021.3:p.Phe273del
ENST00000371953.7:c.818_820del	ENSP00000361021.3:p.Phe273del
ENST00000472832.2:c.245_247del	ENSP00000483066.1:p.Phe82del
NM_000314.5:c.818_820del	NP_000305.3:p.Phe273del
NM_000314.6:c.818_820del	NP_000305.3:p.Phe273del
NM_001304717.2:c.1337_1339del	NP_001291646.2:p.Phe446del
NM_001304718.1:c.227_229del	NP_001291647.1:p.Phe76del
XM_006717926.2:c.773_775del	XP_006717989.1:p.Phe258del
XM_011539981.1:c.818_820del	XP_011538283.1:p.Phe273del
XM_011539982.1:c.722_724del	XP_011538284.1:p.Phe241del
XR_945791.1:n.1388_1390del
NM_000314.7:c.818_820del	NP_000305.3:p.Phe273del
NM_001304717.5:c.1337_1339del	NP_001291646.4:p.Phe446del
NM_001304718.2:c.227_229del	NP_001291647.1:p.Phe76del
NM_000314.8:c.818_820del MANE Select	NP_000305.3:p.Phe273del