Canonical Allele Identifier: CA1926190120

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961100C= , CM000672.2:g.87961100C=	GRCh38
NC_000010.10:g.89720857C= , CM000672.1:g.89720857C=	GRCh37
NC_000010.9:g.89710837C=	NCBI36
NG_007466.2:g.102662C= , LRG_311:g.102662C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1101C=	ENSP00000514759.2:p.Tyr367=
ENST00000710265.1:c.1008C=	ENSP00000518161.1:p.Tyr336=
ENST00000472832.3:c.1008C=	ENSP00000483066.2:p.Tyr336=
ENST00000688158.2:n.1743C=
ENST00000688922.2:c.*838C=	ENSP00000508742.2:n.*838C=
ENST00000700021.1:c.963C=	ENSP00000514757.1:p.Tyr321=
ENST00000700022.1:c.*347C=	ENSP00000514758.1:n.*347C=
ENST00000700023.1:n.2166C=
ENST00000700024.1:n.2400C=
ENST00000700025.1:n.1777C=
ENST00000700026.1:n.645C=
ENST00000706954.1:c.1008C=	ENSP00000516674.1:p.Tyr336=
ENST00000706955.1:c.*1043C=	ENSP00000516675.1:n.*1043C=
ENST00000686459.1:c.*594C=	ENSP00000508909.1:n.*594C=
ENST00000688158.1:c.*1119C=	ENSP00000509254.1:n.*1119C=
ENST00000688308.1:c.1008C=	ENSP00000508752.1:p.Tyr336=
ENST00000688922.1:c.929C=
ENST00000693560.1:c.1527C=	ENSP00000509861.1:p.Tyr509=
ENST00000371953.8:c.1008C= MANE Select	ENSP00000361021.3:p.Tyr336=
ENST00000371953.7:c.1008C=	ENSP00000361021.3:p.Tyr336=
ENST00000472832.2:c.435C=	ENSP00000483066.1:p.Tyr145=
NM_000314.5:c.1008C=	NP_000305.3:p.Tyr336=
NM_000314.6:c.1008C=	NP_000305.3:p.Tyr336=
NM_001304717.2:c.1527C=	NP_001291646.2:p.Tyr509=
NM_001304718.1:c.417C=	NP_001291647.1:p.Tyr139=
XM_006717926.2:c.963C=	XP_006717989.1:p.Tyr321=
XM_011539981.1:c.1008C=	XP_011538283.1:p.Tyr336=
XM_011539982.1:c.912C=	XP_011538284.1:p.Tyr304=
XR_945791.1:n.1578C=
NM_000314.7:c.1008C=	NP_000305.3:p.Tyr336=
NM_001304717.5:c.1527C=	NP_001291646.4:p.Tyr509=
NM_001304718.2:c.417C=	NP_001291647.1:p.Tyr139=
NM_000314.8:c.1008C= MANE Select	NP_000305.3:p.Tyr336=