Canonical Allele Identifier: CA377486118

Gene: PTEN

Linked Data

• COSMIC: COSM133160
• MyVariant Identifiers: chr10:g.89720849A>T (hg19) ; chr10:g.87961092A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961092A>T , CM000672.2:g.87961092A>T	GRCh38
NC_000010.10:g.89720849A>T , CM000672.1:g.89720849A>T	GRCh37
NC_000010.9:g.89710829A>T	NCBI36
NG_007466.2:g.102654A>T , LRG_311:g.102654A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1093A>T	ENSP00000514759.2:p.Asn365Tyr
ENST00000710265.1:c.1000A>T	ENSP00000518161.1:p.Asn334Tyr
ENST00000472832.3:c.1000A>T	ENSP00000483066.2:p.Asn334Tyr
ENST00000688158.2:n.1735A>T
ENST00000688922.2:c.*830A>T	ENSP00000508742.2:n.*830A>T
ENST00000700021.1:c.955A>T	ENSP00000514757.1:p.Asn319Tyr
ENST00000700022.1:c.*339A>T	ENSP00000514758.1:n.*339A>T
ENST00000700023.1:n.2158A>T
ENST00000700024.1:n.2392A>T
ENST00000700025.1:n.1769A>T
ENST00000700026.1:n.637A>T
ENST00000706954.1:c.1000A>T	ENSP00000516674.1:p.Asn334Tyr
ENST00000706955.1:c.*1035A>T	ENSP00000516675.1:n.*1035A>T
ENST00000686459.1:c.*586A>T	ENSP00000508909.1:n.*586A>T
ENST00000688158.1:c.*1111A>T	ENSP00000509254.1:n.*1111A>T
ENST00000688308.1:c.1000A>T	ENSP00000508752.1:p.Asn334Tyr
ENST00000688922.1:c.921A>T
ENST00000693560.1:c.1519A>T	ENSP00000509861.1:p.Asn507Tyr
ENST00000371953.8:c.1000A>T MANE Select	ENSP00000361021.3:p.Asn334Tyr
ENST00000371953.7:c.1000A>T	ENSP00000361021.3:p.Asn334Tyr
ENST00000472832.2:c.427A>T	ENSP00000483066.1:p.Asn143Tyr
NM_000314.5:c.1000A>T	NP_000305.3:p.Asn334Tyr
NM_000314.6:c.1000A>T	NP_000305.3:p.Asn334Tyr
NM_001304717.2:c.1519A>T	NP_001291646.2:p.Asn507Tyr
NM_001304718.1:c.409A>T	NP_001291647.1:p.Asn137Tyr
XM_006717926.2:c.955A>T	XP_006717989.1:p.Asn319Tyr
XM_011539981.1:c.1000A>T	XP_011538283.1:p.Asn334Tyr
XM_011539982.1:c.904A>T	XP_011538284.1:p.Asn302Tyr
XR_945791.1:n.1570A>T
NM_000314.7:c.1000A>T	NP_000305.3:p.Asn334Tyr
NM_001304717.5:c.1519A>T	NP_001291646.4:p.Asn507Tyr
NM_001304718.2:c.409A>T	NP_001291647.1:p.Asn137Tyr
NM_000314.8:c.1000A>T MANE Select	NP_000305.3:p.Asn334Tyr