Canonical Allele Identifier: CA1926190146

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961138T= , CM000672.2:g.87961138T=	GRCh38
NC_000010.10:g.89720895T= , CM000672.1:g.89720895T=	GRCh37
NC_000010.9:g.89710875T=	NCBI36
NG_007466.2:g.102700T= , LRG_311:g.102700T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1119+20T=	ENSP00000514759.2:n.1119+20T=
ENST00000710265.1:c.1026+20T=	ENSP00000518161.1:n.1026+20T=
ENST00000472832.3:c.*11T=	ENSP00000483066.2:n.*11T=
ENST00000688158.2:n.1761+20T=
ENST00000688922.2:c.*856+20T=	ENSP00000508742.2:n.*856+20T=
ENST00000700021.1:c.981+20T=	ENSP00000514757.1:n.981+20T=
ENST00000700022.1:c.*365+20T=	ENSP00000514758.1:n.*365+20T=
ENST00000700023.1:n.2184+20T=
ENST00000700024.1:n.2418+20T=
ENST00000700025.1:n.1815T=
ENST00000700026.1:n.683T=
ENST00000706954.1:c.1026+20T=	ENSP00000516674.1:n.1026+20T=
ENST00000706955.1:c.*1061+20T=	ENSP00000516675.1:n.*1061+20T=
ENST00000686459.1:c.*612+20T=	ENSP00000508909.1:n.*612+20T=
ENST00000688158.1:c.*1137+20T=	ENSP00000509254.1:n.*1137+20T=
ENST00000688308.1:c.1026+20T=	ENSP00000508752.1:n.1026+20T=
ENST00000688922.1:c.947+20T=
ENST00000693560.1:c.1545+20T=	ENSP00000509861.1:n.1545+20T=
ENST00000371953.8:c.1026+20T= MANE Select	ENSP00000361021.3:n.1026+20T=
ENST00000371953.7:c.1026+20T=	ENSP00000361021.3:n.1026+20T=
ENST00000472832.2:c.473T=	ENSP00000483066.1:n.473T=
NM_000314.5:c.1026+20T=	NP_000305.3:n.1026+20T=
NM_000314.6:c.1026+20T=	NP_000305.3:n.1026+20T=
NM_001304717.2:c.1545+20T=	NP_001291646.2:n.1545+20T=
NM_001304718.1:c.435+20T=	NP_001291647.1:n.435+20T=
XM_006717926.2:c.981+20T=	XP_006717989.1:n.981+20T=
XM_011539981.1:c.1026+20T=	XP_011538283.1:n.1026+20T=
XM_011539982.1:c.930+20T=	XP_011538284.1:n.930+20T=
XR_945791.1:n.1596+20T=
NM_000314.7:c.1026+20T=	NP_000305.3:n.1026+20T=
NM_001304717.5:c.1545+20T=	NP_001291646.4:n.1545+20T=
NM_001304718.2:c.435+20T=	NP_001291647.1:n.435+20T=
NM_000314.8:c.1026+20T= MANE Select	NP_000305.3:n.1026+20T=