Canonical Allele Identifier: CA470669247

Gene: PTEN

Linked Data

• dbSNP Id: rs1554825165
• COSMIC: COSM1717477
• MyVariant Identifiers: chr10:g.89717629C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957872C>T , CM000672.2:g.87957872C>T	GRCh38
NC_000010.10:g.89717629C>T , CM000672.1:g.89717629C>T	GRCh37
NC_000010.9:g.89707609C>T	NCBI36
NG_007466.2:g.99434C>T , LRG_311:g.99434C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.654C>T	ENSP00000514759.2:p.Cys218=
ENST00000710265.1:c.654C>T	ENSP00000518161.1:p.Cys218=
ENST00000472832.3:c.654C>T	ENSP00000483066.2:p.Cys218=
ENST00000688158.2:n.1389C>T
ENST00000688922.2:c.*484C>T	ENSP00000508742.2:n.*484C>T
ENST00000700021.1:c.609C>T	ENSP00000514757.1:p.Cys203=
ENST00000700022.1:c.512C>T	ENSP00000514758.1:p.Ala171Val
ENST00000700023.1:n.1812C>T
ENST00000700024.1:n.2046C>T
ENST00000700025.1:n.1423C>T
ENST00000700026.1:n.291C>T
ENST00000700029.1:c.488C>T
ENST00000706954.1:c.654C>T	ENSP00000516674.1:p.Cys218=
ENST00000706955.1:c.*689C>T	ENSP00000516675.1:n.*689C>T
ENST00000686459.1:c.*240C>T	ENSP00000508909.1:n.*240C>T
ENST00000688158.1:c.*765C>T	ENSP00000509254.1:n.*765C>T
ENST00000688308.1:c.654C>T	ENSP00000508752.1:p.Cys218=
ENST00000688922.1:c.575C>T
ENST00000693560.1:c.1173C>T	ENSP00000509861.1:p.Cys391=
ENST00000371953.8:c.654C>T MANE Select	ENSP00000361021.3:p.Cys218=
ENST00000371953.7:c.654C>T	ENSP00000361021.3:p.Cys218=
ENST00000472832.2:c.81C>T	ENSP00000483066.1:p.Cys27=
NM_000314.5:c.654C>T	NP_000305.3:p.Cys218=
NM_000314.6:c.654C>T	NP_000305.3:p.Cys218=
NM_001304717.2:c.1173C>T	NP_001291646.2:p.Cys391=
NM_001304718.1:c.63C>T	NP_001291647.1:p.Cys21=
XM_006717926.2:c.609C>T	XP_006717989.1:p.Cys203=
XM_011539981.1:c.654C>T	XP_011538283.1:p.Cys218=
XM_011539982.1:c.558C>T	XP_011538284.1:p.Cys186=
XR_945791.1:n.1224C>T
NM_000314.7:c.654C>T	NP_000305.3:p.Cys218=
NM_001304717.5:c.1173C>T	NP_001291646.4:p.Cys391=
NM_001304718.2:c.63C>T	NP_001291647.1:p.Cys21=
NM_000314.8:c.654C>T MANE Select	NP_000305.3:p.Cys218=