Canonical Allele Identifier: CA470671460

Gene: PTEN

Linked Data

• dbSNP Id: rs2132290055
• MyVariant Identifiers: chr10:g.89725166T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965409T>A , CM000672.2:g.87965409T>A	GRCh38
NC_000010.10:g.89725166T>A , CM000672.1:g.89725166T>A	GRCh37
NC_000010.9:g.89715146T>A	NCBI36
NG_007466.2:g.106971T>A , LRG_311:g.106971T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1242T>A	ENSP00000514759.2:p.Thr414=
ENST00000710265.1:c.*178T>A	ENSP00000518161.1:n.*178T>A
ENST00000688158.2:n.1884T>A
ENST00000688922.2:c.*979T>A	ENSP00000508742.2:n.*979T>A
ENST00000700021.1:c.1104T>A	ENSP00000514757.1:p.Thr368=
ENST00000700022.1:c.*488T>A	ENSP00000514758.1:n.*488T>A
ENST00000700023.1:n.2307T>A
ENST00000700024.1:n.2541T>A
ENST00000706954.1:c.1149T>A	ENSP00000516674.1:p.Thr383=
ENST00000706955.1:c.*1184T>A	ENSP00000516675.1:n.*1184T>A
ENST00000686459.1:c.*735T>A	ENSP00000508909.1:n.*735T>A
ENST00000688158.1:c.*1260T>A	ENSP00000509254.1:n.*1260T>A
ENST00000688308.1:c.1149T>A	ENSP00000508752.1:p.Thr383=
ENST00000688922.1:c.1070T>A
ENST00000693560.1:c.1668T>A	ENSP00000509861.1:p.Thr556=
ENST00000371953.8:c.1149T>A MANE Select	ENSP00000361021.3:p.Thr383=
ENST00000371953.7:c.1149T>A	ENSP00000361021.3:p.Thr383=
NM_000314.5:c.1149T>A	NP_000305.3:p.Thr383=
NM_000314.6:c.1149T>A	NP_000305.3:p.Thr383=
NM_001304717.2:c.1668T>A	NP_001291646.2:p.Thr556=
NM_001304718.1:c.558T>A	NP_001291647.1:p.Thr186=
XM_006717926.2:c.1104T>A	XP_006717989.1:p.Thr368=
XM_011539982.1:c.1053T>A	XP_011538284.1:p.Thr351=
XR_945791.1:n.1719T>A
NM_000314.7:c.1149T>A	NP_000305.3:p.Thr383=
NM_001304717.5:c.1668T>A	NP_001291646.4:p.Thr556=
NM_001304718.2:c.558T>A	NP_001291647.1:p.Thr186=
NM_000314.8:c.1149T>A MANE Select	NP_000305.3:p.Thr383=