Canonical Allele Identifier: CA1926172955

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965114C= , CM000672.2:g.87965114C=	GRCh38
NC_000010.10:g.89724871C= , CM000672.1:g.89724871C=	GRCh37
NC_000010.9:g.89714851C=	NCBI36
NG_007466.2:g.106676C= , LRG_311:g.106676C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1120-173C=	ENSP00000514759.2:n.1120-173C=
ENST00000710265.1:c.*56-173C=	ENSP00000518161.1:n.*56-173C=
ENST00000688158.2:n.1762-173C=
ENST00000688922.2:c.*857-173C=	ENSP00000508742.2:n.*857-173C=
ENST00000700021.1:c.982-173C=	ENSP00000514757.1:n.982-173C=
ENST00000700022.1:c.*366-173C=	ENSP00000514758.1:n.*366-173C=
ENST00000700023.1:n.2185-173C=
ENST00000700024.1:n.2419-173C=
ENST00000706954.1:c.1027-173C=	ENSP00000516674.1:n.1027-173C=
ENST00000706955.1:c.*1062-173C=	ENSP00000516675.1:n.*1062-173C=
ENST00000686459.1:c.*613-173C=	ENSP00000508909.1:n.*613-173C=
ENST00000688158.1:c.*1138-173C=	ENSP00000509254.1:n.*1138-173C=
ENST00000688308.1:c.1027-173C=	ENSP00000508752.1:n.1027-173C=
ENST00000688922.1:c.948-173C=
ENST00000693560.1:c.1546-173C=	ENSP00000509861.1:n.1546-173C=
ENST00000371953.8:c.1027-173C= MANE Select	ENSP00000361021.3:n.1027-173C=
ENST00000371953.7:c.1027-173C=	ENSP00000361021.3:n.1027-173C=
NM_000314.5:c.1027-173C=	NP_000305.3:n.1027-173C=
NM_000314.6:c.1027-173C=	NP_000305.3:n.1027-173C=
NM_001304717.2:c.1546-173C=	NP_001291646.2:n.1546-173C=
NM_001304718.1:c.436-173C=	NP_001291647.1:n.436-173C=
XM_006717926.2:c.982-173C=	XP_006717989.1:n.982-173C=
XM_011539982.1:c.931-173C=	XP_011538284.1:n.931-173C=
XR_945791.1:n.1597-173C=
NM_000314.7:c.1027-173C=	NP_000305.3:n.1027-173C=
NM_001304717.5:c.1546-173C=	NP_001291646.4:n.1546-173C=
NM_001304718.2:c.436-173C=	NP_001291647.1:n.436-173C=
NM_000314.8:c.1027-173C= MANE Select	NP_000305.3:n.1027-173C=