Canonical Allele Identifier: CA377487436

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725198A>T (hg19) ; chr10:g.87965441A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965441A>T , CM000672.2:g.87965441A>T	GRCh38
NC_000010.10:g.89725198A>T , CM000672.1:g.89725198A>T	GRCh37
NC_000010.9:g.89715178A>T	NCBI36
NG_007466.2:g.107003A>T , LRG_311:g.107003A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1274A>T	ENSP00000514759.2:p.Glu425Val
ENST00000710265.1:c.*210A>T	ENSP00000518161.1:n.*210A>T
ENST00000688158.2:n.1916A>T
ENST00000688922.2:c.*1011A>T	ENSP00000508742.2:n.*1011A>T
ENST00000700021.1:c.1136A>T	ENSP00000514757.1:p.Glu379Val
ENST00000700022.1:c.*520A>T	ENSP00000514758.1:n.*520A>T
ENST00000700023.1:n.2339A>T
ENST00000700024.1:n.2573A>T
ENST00000706954.1:c.1181A>T	ENSP00000516674.1:p.Glu394Val
ENST00000706955.1:c.*1216A>T	ENSP00000516675.1:n.*1216A>T
ENST00000686459.1:c.*767A>T	ENSP00000508909.1:n.*767A>T
ENST00000688158.1:c.*1292A>T	ENSP00000509254.1:n.*1292A>T
ENST00000688308.1:c.1181A>T	ENSP00000508752.1:p.Glu394Val
ENST00000688922.1:c.1102A>T
ENST00000693560.1:c.1700A>T	ENSP00000509861.1:p.Glu567Val
ENST00000371953.8:c.1181A>T MANE Select	ENSP00000361021.3:p.Glu394Val
ENST00000371953.7:c.1181A>T	ENSP00000361021.3:p.Glu394Val
NM_000314.5:c.1181A>T	NP_000305.3:p.Glu394Val
NM_000314.6:c.1181A>T	NP_000305.3:p.Glu394Val
NM_001304717.2:c.1700A>T	NP_001291646.2:p.Glu567Val
NM_001304718.1:c.590A>T	NP_001291647.1:p.Glu197Val
XM_006717926.2:c.1136A>T	XP_006717989.1:p.Glu379Val
XM_011539982.1:c.1085A>T	XP_011538284.1:p.Glu362Val
XR_945791.1:n.1751A>T
NM_000314.7:c.1181A>T	NP_000305.3:p.Glu394Val
NM_001304717.5:c.1700A>T	NP_001291646.4:p.Glu567Val
NM_001304718.2:c.590A>T	NP_001291647.1:p.Glu197Val
NM_000314.8:c.1181A>T MANE Select	NP_000305.3:p.Glu394Val