Canonical Allele Identifier: CA1926189954

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960913G= , CM000672.2:g.87960913G=	GRCh38
NC_000010.10:g.89720670G= , CM000672.1:g.89720670G=	GRCh37
NC_000010.9:g.89710650G=	NCBI36
NG_007466.2:g.102475G= , LRG_311:g.102475G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.914G=	ENSP00000514759.2:p.Trp305=
ENST00000710265.1:c.821G=	ENSP00000518161.1:p.Trp274=
ENST00000472832.3:c.821G=	ENSP00000483066.2:p.Trp274=
ENST00000688158.2:n.1556G=
ENST00000688922.2:c.*651G=	ENSP00000508742.2:n.*651G=
ENST00000700021.1:c.776G=	ENSP00000514757.1:p.Trp259=
ENST00000700022.1:c.*160G=	ENSP00000514758.1:n.*160G=
ENST00000700023.1:n.1979G=
ENST00000700024.1:n.2213G=
ENST00000700025.1:n.1590G=
ENST00000700026.1:n.458G=
ENST00000700029.1:c.748G=
ENST00000706954.1:c.821G=	ENSP00000516674.1:p.Trp274=
ENST00000706955.1:c.*856G=	ENSP00000516675.1:n.*856G=
ENST00000686459.1:c.*407G=	ENSP00000508909.1:n.*407G=
ENST00000688158.1:c.*932G=	ENSP00000509254.1:n.*932G=
ENST00000688308.1:c.821G=	ENSP00000508752.1:p.Trp274=
ENST00000688922.1:c.742G=
ENST00000693560.1:c.1340G=	ENSP00000509861.1:p.Trp447=
ENST00000371953.8:c.821G= MANE Select	ENSP00000361021.3:p.Trp274=
ENST00000371953.7:c.821G=	ENSP00000361021.3:p.Trp274=
ENST00000472832.2:c.248G=	ENSP00000483066.1:p.Trp83=
NM_000314.5:c.821G=	NP_000305.3:p.Trp274=
NM_000314.6:c.821G=	NP_000305.3:p.Trp274=
NM_001304717.2:c.1340G=	NP_001291646.2:p.Trp447=
NM_001304718.1:c.230G=	NP_001291647.1:p.Trp77=
XM_006717926.2:c.776G=	XP_006717989.1:p.Trp259=
XM_011539981.1:c.821G=	XP_011538283.1:p.Trp274=
XM_011539982.1:c.725G=	XP_011538284.1:p.Trp242=
XR_945791.1:n.1391G=
NM_000314.7:c.821G=	NP_000305.3:p.Trp274=
NM_001304717.5:c.1340G=	NP_001291646.4:p.Trp447=
NM_001304718.2:c.230G=	NP_001291647.1:p.Trp77=
NM_000314.8:c.821G= MANE Select	NP_000305.3:p.Trp274=