Canonical Allele Identifier: CA1926174349

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933067C= , CM000672.2:g.87933067C=	GRCh38
NC_000010.10:g.89692824C= , CM000672.1:g.89692824C=	GRCh37
NC_000010.9:g.89682804C=	NCBI36
NG_007466.2:g.74629C= , LRG_311:g.74629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.308C=	ENSP00000514759.2:p.Pro103=
ENST00000710265.1:c.308C=	ENSP00000518161.1:p.Pro103=
ENST00000472832.3:c.308C=	ENSP00000483066.2:p.Pro103=
ENST00000688158.2:n.1043C=
ENST00000688922.2:c.*138C=	ENSP00000508742.2:n.*138C=
ENST00000700021.1:c.263C=	ENSP00000514757.1:p.Pro88=
ENST00000700022.1:c.308C=	ENSP00000514758.1:p.Pro103=
ENST00000700029.1:c.142C=
ENST00000706954.1:c.308C=	ENSP00000516674.1:p.Pro103=
ENST00000706955.1:c.*343C=	ENSP00000516675.1:n.*343C=
ENST00000686459.1:c.308C=	ENSP00000508909.1:p.Pro103=
ENST00000688158.1:c.*419C=	ENSP00000509254.1:n.*419C=
ENST00000688308.1:c.308C=	ENSP00000508752.1:p.Pro103=
ENST00000688922.1:c.229C=
ENST00000693560.1:c.827C=	ENSP00000509861.1:p.Pro276=
ENST00000371953.8:c.308C= MANE Select	ENSP00000361021.3:p.Pro103=
ENST00000371953.7:c.308C=	ENSP00000361021.3:p.Pro103=
ENST00000498703.1:n.134C=
ENST00000610634.1:c.206C=	ENSP00000477517.1:p.Pro69=
NM_000314.5:c.308C=	NP_000305.3:p.Pro103=
NM_000314.6:c.308C=	NP_000305.3:p.Pro103=
NM_001304717.2:c.827C=	NP_001291646.2:p.Pro276=
NM_001304718.1:c.-443C=	NP_001291647.1:n.-443C=
XM_006717926.2:c.263C=	XP_006717989.1:p.Pro88=
XM_011539981.1:c.308C=	XP_011538283.1:p.Pro103=
XM_011539982.1:c.212C=	XP_011538284.1:p.Pro71=
XR_945789.1:n.1020C=
XR_945790.1:n.1020C=
XR_945791.1:n.1020C=
NM_000314.7:c.308C=	NP_000305.3:p.Pro103=
NM_001304717.5:c.827C=	NP_001291646.4:p.Pro276=
NM_001304718.2:c.-443C=	NP_001291647.1:n.-443C=
NM_000314.8:c.308C= MANE Select	NP_000305.3:p.Pro103=