Canonical Allele Identifier: CA1926188515

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957879A= , CM000672.2:g.87957879A=	GRCh38
NC_000010.10:g.89717636A= , CM000672.1:g.89717636A=	GRCh37
NC_000010.9:g.89707616A=	NCBI36
NG_007466.2:g.99441A= , LRG_311:g.99441A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.661A=	ENSP00000514759.2:p.Lys221=
ENST00000710265.1:c.661A=	ENSP00000518161.1:p.Lys221=
ENST00000472832.3:c.661A=	ENSP00000483066.2:p.Lys221=
ENST00000688158.2:n.1396A=
ENST00000688922.2:c.*491A=	ENSP00000508742.2:n.*491A=
ENST00000700021.1:c.616A=	ENSP00000514757.1:p.Lys206=
ENST00000700022.1:c.519A=	ENSP00000514758.1:p.Ter173=
ENST00000700023.1:n.1819A=
ENST00000700024.1:n.2053A=
ENST00000700025.1:n.1430A=
ENST00000700026.1:n.298A=
ENST00000700029.1:c.495A=
ENST00000706954.1:c.661A=	ENSP00000516674.1:p.Lys221=
ENST00000706955.1:c.*696A=	ENSP00000516675.1:n.*696A=
ENST00000686459.1:c.*247A=	ENSP00000508909.1:n.*247A=
ENST00000688158.1:c.*772A=	ENSP00000509254.1:n.*772A=
ENST00000688308.1:c.661A=	ENSP00000508752.1:p.Lys221=
ENST00000688922.1:c.582A=
ENST00000693560.1:c.1180A=	ENSP00000509861.1:p.Lys394=
ENST00000371953.8:c.661A= MANE Select	ENSP00000361021.3:p.Lys221=
ENST00000371953.7:c.661A=	ENSP00000361021.3:p.Lys221=
ENST00000472832.2:c.88A=	ENSP00000483066.1:p.Lys30=
NM_000314.5:c.661A=	NP_000305.3:p.Lys221=
NM_000314.6:c.661A=	NP_000305.3:p.Lys221=
NM_001304717.2:c.1180A=	NP_001291646.2:p.Lys394=
NM_001304718.1:c.70A=	NP_001291647.1:p.Lys24=
XM_006717926.2:c.616A=	XP_006717989.1:p.Lys206=
XM_011539981.1:c.661A=	XP_011538283.1:p.Lys221=
XM_011539982.1:c.565A=	XP_011538284.1:p.Lys189=
XR_945791.1:n.1231A=
NM_000314.7:c.661A=	NP_000305.3:p.Lys221=
NM_001304717.5:c.1180A=	NP_001291646.4:p.Lys394=
NM_001304718.2:c.70A=	NP_001291647.1:p.Lys24=
NM_000314.8:c.661A= MANE Select	NP_000305.3:p.Lys221=