Canonical Allele Identifier: CA1926189947

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960904T= , CM000672.2:g.87960904T=	GRCh38
NC_000010.10:g.89720661T= , CM000672.1:g.89720661T=	GRCh37
NC_000010.9:g.89710641T=	NCBI36
NG_007466.2:g.102466T= , LRG_311:g.102466T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.905T=	ENSP00000514759.2:p.Phe302=
ENST00000710265.1:c.812T=	ENSP00000518161.1:p.Phe271=
ENST00000472832.3:c.812T=	ENSP00000483066.2:p.Phe271=
ENST00000688158.2:n.1547T=
ENST00000688922.2:c.*642T=	ENSP00000508742.2:n.*642T=
ENST00000700021.1:c.767T=	ENSP00000514757.1:p.Phe256=
ENST00000700022.1:c.*151T=	ENSP00000514758.1:n.*151T=
ENST00000700023.1:n.1970T=
ENST00000700024.1:n.2204T=
ENST00000700025.1:n.1581T=
ENST00000700026.1:n.449T=
ENST00000700029.1:c.739T=
ENST00000706954.1:c.812T=	ENSP00000516674.1:p.Phe271=
ENST00000706955.1:c.*847T=	ENSP00000516675.1:n.*847T=
ENST00000686459.1:c.*398T=	ENSP00000508909.1:n.*398T=
ENST00000688158.1:c.*923T=	ENSP00000509254.1:n.*923T=
ENST00000688308.1:c.812T=	ENSP00000508752.1:p.Phe271=
ENST00000688922.1:c.733T=
ENST00000693560.1:c.1331T=	ENSP00000509861.1:p.Phe444=
ENST00000371953.8:c.812T= MANE Select	ENSP00000361021.3:p.Phe271=
ENST00000371953.7:c.812T=	ENSP00000361021.3:p.Phe271=
ENST00000472832.2:c.239T=	ENSP00000483066.1:p.Phe80=
NM_000314.5:c.812T=	NP_000305.3:p.Phe271=
NM_000314.6:c.812T=	NP_000305.3:p.Phe271=
NM_001304717.2:c.1331T=	NP_001291646.2:p.Phe444=
NM_001304718.1:c.221T=	NP_001291647.1:p.Phe74=
XM_006717926.2:c.767T=	XP_006717989.1:p.Phe256=
XM_011539981.1:c.812T=	XP_011538283.1:p.Phe271=
XM_011539982.1:c.716T=	XP_011538284.1:p.Phe239=
XR_945791.1:n.1382T=
NM_000314.7:c.812T=	NP_000305.3:p.Phe271=
NM_001304717.5:c.1331T=	NP_001291646.4:p.Phe444=
NM_001304718.2:c.221T=	NP_001291647.1:p.Phe74=
NM_000314.8:c.812T= MANE Select	NP_000305.3:p.Phe271=