Canonical Allele Identifier: CA1926174057

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965448G= , CM000672.2:g.87965448G=	GRCh38
NC_000010.10:g.89725205G= , CM000672.1:g.89725205G=	GRCh37
NC_000010.9:g.89715185G=	NCBI36
NG_007466.2:g.107010G= , LRG_311:g.107010G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1281G=	ENSP00000514759.2:p.Gln427=
ENST00000710265.1:c.*217G=	ENSP00000518161.1:n.*217G=
ENST00000688158.2:n.1923G=
ENST00000688922.2:c.*1018G=	ENSP00000508742.2:n.*1018G=
ENST00000700021.1:c.1143G=	ENSP00000514757.1:p.Gln381=
ENST00000700022.1:c.*527G=	ENSP00000514758.1:n.*527G=
ENST00000700023.1:n.2346G=
ENST00000700024.1:n.2580G=
ENST00000706954.1:c.1188G=	ENSP00000516674.1:p.Gln396=
ENST00000706955.1:c.*1223G=	ENSP00000516675.1:n.*1223G=
ENST00000686459.1:c.*774G=	ENSP00000508909.1:n.*774G=
ENST00000688158.1:c.*1299G=	ENSP00000509254.1:n.*1299G=
ENST00000688308.1:c.1188G=	ENSP00000508752.1:p.Gln396=
ENST00000688922.1:c.1109G=
ENST00000693560.1:c.1707G=	ENSP00000509861.1:p.Gln569=
ENST00000371953.8:c.1188G= MANE Select	ENSP00000361021.3:p.Gln396=
ENST00000371953.7:c.1188G=	ENSP00000361021.3:p.Gln396=
NM_000314.5:c.1188G=	NP_000305.3:p.Gln396=
NM_000314.6:c.1188G=	NP_000305.3:p.Gln396=
NM_001304717.2:c.1707G=	NP_001291646.2:p.Gln569=
NM_001304718.1:c.597G=	NP_001291647.1:p.Gln199=
XM_006717926.2:c.1143G=	XP_006717989.1:p.Gln381=
XM_011539982.1:c.1092G=	XP_011538284.1:p.Gln364=
XR_945791.1:n.1758G=
NM_000314.7:c.1188G=	NP_000305.3:p.Gln396=
NM_001304717.5:c.1707G=	NP_001291646.4:p.Gln569=
NM_001304718.2:c.597G=	NP_001291647.1:p.Gln199=
NM_000314.8:c.1188G= MANE Select	NP_000305.3:p.Gln396=