Canonical Allele Identifier: CA1926156904

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894038C= , CM000672.2:g.87894038C=	GRCh38
NC_000010.10:g.89653795C= , CM000672.1:g.89653795C=	GRCh37
NC_000010.9:g.89643775C=	NCBI36
NG_007466.2:g.35600C= , LRG_311:g.35600C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.93C=	ENSP00000514759.2:p.Asn31=
ENST00000710265.1:c.93C=	ENSP00000518161.1:p.Asn31=
ENST00000472832.3:c.93C=	ENSP00000483066.2:p.Asn31=
ENST00000688158.2:n.899+13600C=
ENST00000688922.2:c.93C=	ENSP00000508742.2:p.Asn31=
ENST00000700021.1:c.93C=	ENSP00000514757.1:p.Asn31=
ENST00000700022.1:c.93C=	ENSP00000514758.1:p.Asn31=
ENST00000706954.1:c.93C=	ENSP00000516674.1:p.Asn31=
ENST00000706955.1:c.*128C=	ENSP00000516675.1:n.*128C=
ENST00000686459.1:c.93C=	ENSP00000508909.1:p.Asn31=
ENST00000688158.1:c.*275+13600C=	ENSP00000509254.1:n.*275+13600C=
ENST00000688308.1:c.93C=	ENSP00000508752.1:p.Asn31=
ENST00000693560.1:c.612C=	ENSP00000509861.1:p.Asn204=
ENST00000371953.8:c.93C= MANE Select	ENSP00000361021.3:p.Asn31=
ENST00000371953.7:c.93C=	ENSP00000361021.3:p.Asn31=
ENST00000462694.1:n.95C=
ENST00000610634.1:c.-10C=	ENSP00000477517.1:n.-10C=
NM_000314.5:c.93C=	NP_000305.3:p.Asn31=
NM_000314.6:c.93C=	NP_000305.3:p.Asn31=
NM_001304717.2:c.612C=	NP_001291646.2:p.Asn204=
NM_001304718.1:c.-613C=	NP_001291647.1:n.-613C=
XM_006717926.2:c.93C=	XP_006717989.1:p.Asn31=
XM_011539981.1:c.93C=	XP_011538283.1:p.Asn31=
XM_011539982.1:c.68+13600C=	XP_011538284.1:n.68+13600C=
XR_945789.1:n.805C=
XR_945790.1:n.805C=
XR_945791.1:n.805C=
NM_000314.7:c.93C=	NP_000305.3:p.Asn31=
NM_001304717.5:c.612C=	NP_001291646.4:p.Asn204=
NM_001304718.2:c.-613C=	NP_001291647.1:n.-613C=
NM_000314.8:c.93C= MANE Select	NP_000305.3:p.Asn31=