Canonical Allele Identifier: CA1926189972

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960935A= , CM000672.2:g.87960935A=	GRCh38
NC_000010.10:g.89720692A= , CM000672.1:g.89720692A=	GRCh37
NC_000010.9:g.89710672A=	NCBI36
NG_007466.2:g.102497A= , LRG_311:g.102497A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.936A=	ENSP00000514759.2:p.Pro312=
ENST00000710265.1:c.843A=	ENSP00000518161.1:p.Pro281=
ENST00000472832.3:c.843A=	ENSP00000483066.2:p.Pro281=
ENST00000688158.2:n.1578A=
ENST00000688922.2:c.*673A=	ENSP00000508742.2:n.*673A=
ENST00000700021.1:c.798A=	ENSP00000514757.1:p.Pro266=
ENST00000700022.1:c.*182A=	ENSP00000514758.1:n.*182A=
ENST00000700023.1:n.2001A=
ENST00000700024.1:n.2235A=
ENST00000700025.1:n.1612A=
ENST00000700026.1:n.480A=
ENST00000700029.1:c.770A=
ENST00000706954.1:c.843A=	ENSP00000516674.1:p.Pro281=
ENST00000706955.1:c.*878A=	ENSP00000516675.1:n.*878A=
ENST00000686459.1:c.*429A=	ENSP00000508909.1:n.*429A=
ENST00000688158.1:c.*954A=	ENSP00000509254.1:n.*954A=
ENST00000688308.1:c.843A=	ENSP00000508752.1:p.Pro281=
ENST00000688922.1:c.764A=
ENST00000693560.1:c.1362A=	ENSP00000509861.1:p.Pro454=
ENST00000371953.8:c.843A= MANE Select	ENSP00000361021.3:p.Pro281=
ENST00000371953.7:c.843A=	ENSP00000361021.3:p.Pro281=
ENST00000472832.2:c.270A=	ENSP00000483066.1:p.Pro90=
NM_000314.5:c.843A=	NP_000305.3:p.Pro281=
NM_000314.6:c.843A=	NP_000305.3:p.Pro281=
NM_001304717.2:c.1362A=	NP_001291646.2:p.Pro454=
NM_001304718.1:c.252A=	NP_001291647.1:p.Pro84=
XM_006717926.2:c.798A=	XP_006717989.1:p.Pro266=
XM_011539981.1:c.843A=	XP_011538283.1:p.Pro281=
XM_011539982.1:c.747A=	XP_011538284.1:p.Pro249=
XR_945791.1:n.1413A=
NM_000314.7:c.843A=	NP_000305.3:p.Pro281=
NM_001304717.5:c.1362A=	NP_001291646.4:p.Pro454=
NM_001304718.2:c.252A=	NP_001291647.1:p.Pro84=
NM_000314.8:c.843A= MANE Select	NP_000305.3:p.Pro281=