Canonical Allele Identifier: CA1926190094

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961064T= , CM000672.2:g.87961064T=	GRCh38
NC_000010.10:g.89720821T= , CM000672.1:g.89720821T=	GRCh37
NC_000010.9:g.89710801T=	NCBI36
NG_007466.2:g.102626T= , LRG_311:g.102626T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1065T=	ENSP00000514759.2:p.Asp355=
ENST00000710265.1:c.972T=	ENSP00000518161.1:p.Asp324=
ENST00000472832.3:c.972T=	ENSP00000483066.2:p.Asp324=
ENST00000688158.2:n.1707T=
ENST00000688922.2:c.*802T=	ENSP00000508742.2:n.*802T=
ENST00000700021.1:c.927T=	ENSP00000514757.1:p.Asp309=
ENST00000700022.1:c.*311T=	ENSP00000514758.1:n.*311T=
ENST00000700023.1:n.2130T=
ENST00000700024.1:n.2364T=
ENST00000700025.1:n.1741T=
ENST00000700026.1:n.609T=
ENST00000706954.1:c.972T=	ENSP00000516674.1:p.Asp324=
ENST00000706955.1:c.*1007T=	ENSP00000516675.1:n.*1007T=
ENST00000686459.1:c.*558T=	ENSP00000508909.1:n.*558T=
ENST00000688158.1:c.*1083T=	ENSP00000509254.1:n.*1083T=
ENST00000688308.1:c.972T=	ENSP00000508752.1:p.Asp324=
ENST00000688922.1:c.893T=
ENST00000693560.1:c.1491T=	ENSP00000509861.1:p.Asp497=
ENST00000371953.8:c.972T= MANE Select	ENSP00000361021.3:p.Asp324=
ENST00000371953.7:c.972T=	ENSP00000361021.3:p.Asp324=
ENST00000472832.2:c.399T=	ENSP00000483066.1:p.Asp133=
NM_000314.5:c.972T=	NP_000305.3:p.Asp324=
NM_000314.6:c.972T=	NP_000305.3:p.Asp324=
NM_001304717.2:c.1491T=	NP_001291646.2:p.Asp497=
NM_001304718.1:c.381T=	NP_001291647.1:p.Asp127=
XM_006717926.2:c.927T=	XP_006717989.1:p.Asp309=
XM_011539981.1:c.972T=	XP_011538283.1:p.Asp324=
XM_011539982.1:c.876T=	XP_011538284.1:p.Asp292=
XR_945791.1:n.1542T=
NM_000314.7:c.972T=	NP_000305.3:p.Asp324=
NM_001304717.5:c.1491T=	NP_001291646.4:p.Asp497=
NM_001304718.2:c.381T=	NP_001291647.1:p.Asp127=
NM_000314.8:c.972T= MANE Select	NP_000305.3:p.Asp324=