Canonical Allele Identifier: CA1926176068

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933223A= , CM000672.2:g.87933223A=	GRCh38
NC_000010.10:g.89692980A= , CM000672.1:g.89692980A=	GRCh37
NC_000010.9:g.89682960A=	NCBI36
NG_007466.2:g.74785A= , LRG_311:g.74785A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.464A= MANE Select	NP_000305.3:p.Tyr155=
ENST00000371953.8:c.464A= MANE Select	ENSP00000361021.3:p.Tyr155=
NM_000314.5:c.464A=	NP_000305.3:p.Tyr155=
NM_000314.6:c.464A=	NP_000305.3:p.Tyr155=
NM_000314.7:c.464A=	NP_000305.3:p.Tyr155=
NM_001304717.2:c.983A=	NP_001291646.2:p.Tyr328=
NM_001304717.5:c.983A=	NP_001291646.4:p.Tyr328=
NM_001304718.1:c.-287A=	NP_001291647.1:n.-287A=
NM_001304718.2:c.-287A=	NP_001291647.1:n.-287A=
ENST00000371953.7:c.464A=	ENSP00000361021.3:p.Tyr155=
ENST00000472832.3:c.464A=	ENSP00000483066.2:p.Tyr155=
ENST00000498703.1:n.290A=
ENST00000610634.1:c.362A=	ENSP00000477517.1:p.Tyr121=
ENST00000686459.1:c.464A=	ENSP00000508909.1:p.Tyr155=
ENST00000688158.1:c.*575A=	ENSP00000509254.1:n.*575A=
ENST00000688158.2:n.1199A=
ENST00000688308.1:c.464A=	ENSP00000508752.1:p.Tyr155=
ENST00000688922.1:c.385A=
ENST00000688922.2:c.*294A=	ENSP00000508742.2:n.*294A=
ENST00000693560.1:c.983A=	ENSP00000509861.1:p.Tyr328=
ENST00000700021.1:c.419A=	ENSP00000514757.1:p.Tyr140=
ENST00000700022.1:c.464A=	ENSP00000514758.1:p.Tyr155=
ENST00000700029.1:c.298A=
ENST00000700029.2:c.464A=	ENSP00000514759.2:p.Tyr155=
ENST00000706954.1:c.464A=	ENSP00000516674.1:p.Tyr155=
ENST00000706955.1:c.*499A=	ENSP00000516675.1:n.*499A=
ENST00000710265.1:c.464A=	ENSP00000518161.1:p.Tyr155=
XM_006717926.2:c.419A=	XP_006717989.1:p.Tyr140=
XM_011539981.1:c.464A=	XP_011538283.1:p.Tyr155=
XM_011539982.1:c.368A=	XP_011538284.1:p.Tyr123=
XR_945789.1:n.1176A=
XR_945790.1:n.1176A=
XR_945791.1:n.1176A=