Canonical Allele Identifier: CA1926189967

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960927T= , CM000672.2:g.87960927T=	GRCh38
NC_000010.10:g.89720684T= , CM000672.1:g.89720684T=	GRCh37
NC_000010.9:g.89710664T=	NCBI36
NG_007466.2:g.102489T= , LRG_311:g.102489T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.928T=	ENSP00000514759.2:p.Phe310=
ENST00000710265.1:c.835T=	ENSP00000518161.1:p.Phe279=
ENST00000472832.3:c.835T=	ENSP00000483066.2:p.Phe279=
ENST00000688158.2:n.1570T=
ENST00000688922.2:c.*665T=	ENSP00000508742.2:n.*665T=
ENST00000700021.1:c.790T=	ENSP00000514757.1:p.Phe264=
ENST00000700022.1:c.*174T=	ENSP00000514758.1:n.*174T=
ENST00000700023.1:n.1993T=
ENST00000700024.1:n.2227T=
ENST00000700025.1:n.1604T=
ENST00000700026.1:n.472T=
ENST00000700029.1:c.762T=
ENST00000706954.1:c.835T=	ENSP00000516674.1:p.Phe279=
ENST00000706955.1:c.*870T=	ENSP00000516675.1:n.*870T=
ENST00000686459.1:c.*421T=	ENSP00000508909.1:n.*421T=
ENST00000688158.1:c.*946T=	ENSP00000509254.1:n.*946T=
ENST00000688308.1:c.835T=	ENSP00000508752.1:p.Phe279=
ENST00000688922.1:c.756T=
ENST00000693560.1:c.1354T=	ENSP00000509861.1:p.Phe452=
ENST00000371953.8:c.835T= MANE Select	ENSP00000361021.3:p.Phe279=
ENST00000371953.7:c.835T=	ENSP00000361021.3:p.Phe279=
ENST00000472832.2:c.262T=	ENSP00000483066.1:p.Phe88=
NM_000314.5:c.835T=	NP_000305.3:p.Phe279=
NM_000314.6:c.835T=	NP_000305.3:p.Phe279=
NM_001304717.2:c.1354T=	NP_001291646.2:p.Phe452=
NM_001304718.1:c.244T=	NP_001291647.1:p.Phe82=
XM_006717926.2:c.790T=	XP_006717989.1:p.Phe264=
XM_011539981.1:c.835T=	XP_011538283.1:p.Phe279=
XM_011539982.1:c.739T=	XP_011538284.1:p.Phe247=
XR_945791.1:n.1405T=
NM_000314.7:c.835T=	NP_000305.3:p.Phe279=
NM_001304717.5:c.1354T=	NP_001291646.4:p.Phe452=
NM_001304718.2:c.244T=	NP_001291647.1:p.Phe82=
NM_000314.8:c.835T= MANE Select	NP_000305.3:p.Phe279=