Canonical Allele Identifier: CA470671116

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725106T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965349T>G , CM000672.2:g.87965349T>G	GRCh38
NC_000010.10:g.89725106T>G , CM000672.1:g.89725106T>G	GRCh37
NC_000010.9:g.89715086T>G	NCBI36
NG_007466.2:g.106911T>G , LRG_311:g.106911T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1182T>G	ENSP00000514759.2:p.Thr394=
ENST00000710265.1:c.*118T>G	ENSP00000518161.1:n.*118T>G
ENST00000688158.2:n.1824T>G
ENST00000688922.2:c.*919T>G	ENSP00000508742.2:n.*919T>G
ENST00000700021.1:c.1044T>G	ENSP00000514757.1:p.Thr348=
ENST00000700022.1:c.*428T>G	ENSP00000514758.1:n.*428T>G
ENST00000700023.1:n.2247T>G
ENST00000700024.1:n.2481T>G
ENST00000706954.1:c.1089T>G	ENSP00000516674.1:p.Thr363=
ENST00000706955.1:c.*1124T>G	ENSP00000516675.1:n.*1124T>G
ENST00000686459.1:c.*675T>G	ENSP00000508909.1:n.*675T>G
ENST00000688158.1:c.*1200T>G	ENSP00000509254.1:n.*1200T>G
ENST00000688308.1:c.1089T>G	ENSP00000508752.1:p.Thr363=
ENST00000688922.1:c.1010T>G
ENST00000693560.1:c.1608T>G	ENSP00000509861.1:p.Thr536=
ENST00000371953.8:c.1089T>G MANE Select	ENSP00000361021.3:p.Thr363=
ENST00000371953.7:c.1089T>G	ENSP00000361021.3:p.Thr363=
NM_000314.5:c.1089T>G	NP_000305.3:p.Thr363=
NM_000314.6:c.1089T>G	NP_000305.3:p.Thr363=
NM_001304717.2:c.1608T>G	NP_001291646.2:p.Thr536=
NM_001304718.1:c.498T>G	NP_001291647.1:p.Thr166=
XM_006717926.2:c.1044T>G	XP_006717989.1:p.Thr348=
XM_011539982.1:c.993T>G	XP_011538284.1:p.Thr331=
XR_945791.1:n.1659T>G
NM_000314.7:c.1089T>G	NP_000305.3:p.Thr363=
NM_001304717.5:c.1608T>G	NP_001291646.4:p.Thr536=
NM_001304718.2:c.498T>G	NP_001291647.1:p.Thr166=
NM_000314.8:c.1089T>G MANE Select	NP_000305.3:p.Thr363=