Canonical Allele Identifier: CA1926190118

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961098T= , CM000672.2:g.87961098T=	GRCh38
NC_000010.10:g.89720855T= , CM000672.1:g.89720855T=	GRCh37
NC_000010.9:g.89710835T=	NCBI36
NG_007466.2:g.102660T= , LRG_311:g.102660T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1099T=	ENSP00000514759.2:p.Tyr367=
ENST00000710265.1:c.1006T=	ENSP00000518161.1:p.Tyr336=
ENST00000472832.3:c.1006T=	ENSP00000483066.2:p.Tyr336=
ENST00000688158.2:n.1741T=
ENST00000688922.2:c.*836T=	ENSP00000508742.2:n.*836T=
ENST00000700021.1:c.961T=	ENSP00000514757.1:p.Tyr321=
ENST00000700022.1:c.*345T=	ENSP00000514758.1:n.*345T=
ENST00000700023.1:n.2164T=
ENST00000700024.1:n.2398T=
ENST00000700025.1:n.1775T=
ENST00000700026.1:n.643T=
ENST00000706954.1:c.1006T=	ENSP00000516674.1:p.Tyr336=
ENST00000706955.1:c.*1041T=	ENSP00000516675.1:n.*1041T=
ENST00000686459.1:c.*592T=	ENSP00000508909.1:n.*592T=
ENST00000688158.1:c.*1117T=	ENSP00000509254.1:n.*1117T=
ENST00000688308.1:c.1006T=	ENSP00000508752.1:p.Tyr336=
ENST00000688922.1:c.927T=
ENST00000693560.1:c.1525T=	ENSP00000509861.1:p.Tyr509=
ENST00000371953.8:c.1006T= MANE Select	ENSP00000361021.3:p.Tyr336=
ENST00000371953.7:c.1006T=	ENSP00000361021.3:p.Tyr336=
ENST00000472832.2:c.433T=	ENSP00000483066.1:p.Tyr145=
NM_000314.5:c.1006T=	NP_000305.3:p.Tyr336=
NM_000314.6:c.1006T=	NP_000305.3:p.Tyr336=
NM_001304717.2:c.1525T=	NP_001291646.2:p.Tyr509=
NM_001304718.1:c.415T=	NP_001291647.1:p.Tyr139=
XM_006717926.2:c.961T=	XP_006717989.1:p.Tyr321=
XM_011539981.1:c.1006T=	XP_011538283.1:p.Tyr336=
XM_011539982.1:c.910T=	XP_011538284.1:p.Tyr304=
XR_945791.1:n.1576T=
NM_000314.7:c.1006T=	NP_000305.3:p.Tyr336=
NM_001304717.5:c.1525T=	NP_001291646.4:p.Tyr509=
NM_001304718.2:c.415T=	NP_001291647.1:p.Tyr139=
NM_000314.8:c.1006T= MANE Select	NP_000305.3:p.Tyr336=