Canonical Allele Identifier: CA1926156818

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894028T= , CM000672.2:g.87894028T=	GRCh38
NC_000010.10:g.89653785T= , CM000672.1:g.89653785T=	GRCh37
NC_000010.9:g.89643765T=	NCBI36
NG_007466.2:g.35590T= , LRG_311:g.35590T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.83T=	ENSP00000514759.2:p.Ile28=
ENST00000710265.1:c.83T=	ENSP00000518161.1:p.Ile28=
ENST00000472832.3:c.83T=	ENSP00000483066.2:p.Ile28=
ENST00000688158.2:n.899+13590T=
ENST00000688922.2:c.83T=	ENSP00000508742.2:p.Ile28=
ENST00000700021.1:c.83T=	ENSP00000514757.1:p.Ile28=
ENST00000700022.1:c.83T=	ENSP00000514758.1:p.Ile28=
ENST00000706954.1:c.83T=	ENSP00000516674.1:p.Ile28=
ENST00000706955.1:c.*118T=	ENSP00000516675.1:n.*118T=
ENST00000686459.1:c.83T=	ENSP00000508909.1:p.Ile28=
ENST00000688158.1:c.*275+13590T=	ENSP00000509254.1:n.*275+13590T=
ENST00000688308.1:c.83T=	ENSP00000508752.1:p.Ile28=
ENST00000693560.1:c.602T=	ENSP00000509861.1:p.Ile201=
ENST00000371953.8:c.83T= MANE Select	ENSP00000361021.3:p.Ile28=
ENST00000371953.7:c.83T=	ENSP00000361021.3:p.Ile28=
ENST00000462694.1:n.85T=
ENST00000610634.1:c.-20T=	ENSP00000477517.1:n.-20T=
NM_000314.5:c.83T=	NP_000305.3:p.Ile28=
NM_000314.6:c.83T=	NP_000305.3:p.Ile28=
NM_001304717.2:c.602T=	NP_001291646.2:p.Ile201=
NM_001304718.1:c.-623T=	NP_001291647.1:n.-623T=
XM_006717926.2:c.83T=	XP_006717989.1:p.Ile28=
XM_011539981.1:c.83T=	XP_011538283.1:p.Ile28=
XM_011539982.1:c.68+13590T=	XP_011538284.1:n.68+13590T=
XR_945789.1:n.795T=
XR_945790.1:n.795T=
XR_945791.1:n.795T=
NM_000314.7:c.83T=	NP_000305.3:p.Ile28=
NM_001304717.5:c.602T=	NP_001291646.4:p.Ile201=
NM_001304718.2:c.-623T=	NP_001291647.1:n.-623T=
NM_000314.8:c.83T= MANE Select	NP_000305.3:p.Ile28=