Canonical Allele Identifier: CA1926173483

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965307A= , CM000672.2:g.87965307A=	GRCh38
NC_000010.10:g.89725064A= , CM000672.1:g.89725064A=	GRCh37
NC_000010.9:g.89715044A=	NCBI36
NG_007466.2:g.106869A= , LRG_311:g.106869A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1140A=	ENSP00000514759.2:p.Lys380=
ENST00000710265.1:c.*76A=	ENSP00000518161.1:n.*76A=
ENST00000688158.2:n.1782A=
ENST00000688922.2:c.*877A=	ENSP00000508742.2:n.*877A=
ENST00000700021.1:c.1002A=	ENSP00000514757.1:p.Lys334=
ENST00000700022.1:c.*386A=	ENSP00000514758.1:n.*386A=
ENST00000700023.1:n.2205A=
ENST00000700024.1:n.2439A=
ENST00000706954.1:c.1047A=	ENSP00000516674.1:p.Lys349=
ENST00000706955.1:c.*1082A=	ENSP00000516675.1:n.*1082A=
ENST00000686459.1:c.*633A=	ENSP00000508909.1:n.*633A=
ENST00000688158.1:c.*1158A=	ENSP00000509254.1:n.*1158A=
ENST00000688308.1:c.1047A=	ENSP00000508752.1:p.Lys349=
ENST00000688922.1:c.968A=
ENST00000693560.1:c.1566A=	ENSP00000509861.1:p.Lys522=
ENST00000371953.8:c.1047A= MANE Select	ENSP00000361021.3:p.Lys349=
ENST00000371953.7:c.1047A=	ENSP00000361021.3:p.Lys349=
NM_000314.5:c.1047A=	NP_000305.3:p.Lys349=
NM_000314.6:c.1047A=	NP_000305.3:p.Lys349=
NM_001304717.2:c.1566A=	NP_001291646.2:p.Lys522=
NM_001304718.1:c.456A=	NP_001291647.1:p.Lys152=
XM_006717926.2:c.1002A=	XP_006717989.1:p.Lys334=
XM_011539982.1:c.951A=	XP_011538284.1:p.Lys317=
XR_945791.1:n.1617A=
NM_000314.7:c.1047A=	NP_000305.3:p.Lys349=
NM_001304717.5:c.1566A=	NP_001291646.4:p.Lys522=
NM_001304718.2:c.456A=	NP_001291647.1:p.Lys152=
NM_000314.8:c.1047A= MANE Select	NP_000305.3:p.Lys349=