Canonical Allele Identifier: CA377487466

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725210C>G (hg19) ; chr10:g.87965453C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965453C>G , CM000672.2:g.87965453C>G	GRCh38
NC_000010.10:g.89725210C>G , CM000672.1:g.89725210C>G	GRCh37
NC_000010.9:g.89715190C>G	NCBI36
NG_007466.2:g.107015C>G , LRG_311:g.107015C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1286C>G	ENSP00000514759.2:p.Thr429Arg
ENST00000710265.1:c.*222C>G	ENSP00000518161.1:n.*222C>G
ENST00000688158.2:n.1928C>G
ENST00000688922.2:c.*1023C>G	ENSP00000508742.2:n.*1023C>G
ENST00000700021.1:c.1148C>G	ENSP00000514757.1:p.Thr383Arg
ENST00000700022.1:c.*532C>G	ENSP00000514758.1:n.*532C>G
ENST00000700023.1:n.2351C>G
ENST00000700024.1:n.2585C>G
ENST00000706954.1:c.1193C>G	ENSP00000516674.1:p.Thr398Arg
ENST00000706955.1:c.*1228C>G	ENSP00000516675.1:n.*1228C>G
ENST00000686459.1:c.*779C>G	ENSP00000508909.1:n.*779C>G
ENST00000688158.1:c.*1304C>G	ENSP00000509254.1:n.*1304C>G
ENST00000688308.1:c.1193C>G	ENSP00000508752.1:p.Thr398Arg
ENST00000688922.1:c.1114C>G
ENST00000693560.1:c.1712C>G	ENSP00000509861.1:p.Thr571Arg
ENST00000371953.8:c.1193C>G MANE Select	ENSP00000361021.3:p.Thr398Arg
ENST00000371953.7:c.1193C>G	ENSP00000361021.3:p.Thr398Arg
NM_000314.5:c.1193C>G	NP_000305.3:p.Thr398Arg
NM_000314.6:c.1193C>G	NP_000305.3:p.Thr398Arg
NM_001304717.2:c.1712C>G	NP_001291646.2:p.Thr571Arg
NM_001304718.1:c.602C>G	NP_001291647.1:p.Thr201Arg
XM_006717926.2:c.1148C>G	XP_006717989.1:p.Thr383Arg
XM_011539982.1:c.1097C>G	XP_011538284.1:p.Thr366Arg
XR_945791.1:n.1763C>G
NM_000314.7:c.1193C>G	NP_000305.3:p.Thr398Arg
NM_001304717.5:c.1712C>G	NP_001291646.4:p.Thr571Arg
NM_001304718.2:c.602C>G	NP_001291647.1:p.Thr201Arg
NM_000314.8:c.1193C>G MANE Select	NP_000305.3:p.Thr398Arg