Canonical Allele Identifier: CA470671340

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725139T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965382T>G , CM000672.2:g.87965382T>G	GRCh38
NC_000010.10:g.89725139T>G , CM000672.1:g.89725139T>G	GRCh37
NC_000010.9:g.89715119T>G	NCBI36
NG_007466.2:g.106944T>G , LRG_311:g.106944T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1215T>G	ENSP00000514759.2:p.Pro405=
ENST00000710265.1:c.*151T>G	ENSP00000518161.1:n.*151T>G
ENST00000688158.2:n.1857T>G
ENST00000688922.2:c.*952T>G	ENSP00000508742.2:n.*952T>G
ENST00000700021.1:c.1077T>G	ENSP00000514757.1:p.Pro359=
ENST00000700022.1:c.*461T>G	ENSP00000514758.1:n.*461T>G
ENST00000700023.1:n.2280T>G
ENST00000700024.1:n.2514T>G
ENST00000706954.1:c.1122T>G	ENSP00000516674.1:p.Pro374=
ENST00000706955.1:c.*1157T>G	ENSP00000516675.1:n.*1157T>G
ENST00000686459.1:c.*708T>G	ENSP00000508909.1:n.*708T>G
ENST00000688158.1:c.*1233T>G	ENSP00000509254.1:n.*1233T>G
ENST00000688308.1:c.1122T>G	ENSP00000508752.1:p.Pro374=
ENST00000688922.1:c.1043T>G
ENST00000693560.1:c.1641T>G	ENSP00000509861.1:p.Pro547=
ENST00000371953.8:c.1122T>G MANE Select	ENSP00000361021.3:p.Pro374=
ENST00000371953.7:c.1122T>G	ENSP00000361021.3:p.Pro374=
NM_000314.5:c.1122T>G	NP_000305.3:p.Pro374=
NM_000314.6:c.1122T>G	NP_000305.3:p.Pro374=
NM_001304717.2:c.1641T>G	NP_001291646.2:p.Pro547=
NM_001304718.1:c.531T>G	NP_001291647.1:p.Pro177=
XM_006717926.2:c.1077T>G	XP_006717989.1:p.Pro359=
XM_011539982.1:c.1026T>G	XP_011538284.1:p.Pro342=
XR_945791.1:n.1692T>G
NM_000314.7:c.1122T>G	NP_000305.3:p.Pro374=
NM_001304717.5:c.1641T>G	NP_001291646.4:p.Pro547=
NM_001304718.2:c.531T>G	NP_001291647.1:p.Pro177=
NM_000314.8:c.1122T>G MANE Select	NP_000305.3:p.Pro374=