Canonical Allele Identifier: CA470671061

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725094T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965337T>G , CM000672.2:g.87965337T>G	GRCh38
NC_000010.10:g.89725094T>G , CM000672.1:g.89725094T>G	GRCh37
NC_000010.9:g.89715074T>G	NCBI36
NG_007466.2:g.106899T>G , LRG_311:g.106899T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1170T>G	ENSP00000514759.2:p.Ala390=
ENST00000710265.1:c.*106T>G	ENSP00000518161.1:n.*106T>G
ENST00000688158.2:n.1812T>G
ENST00000688922.2:c.*907T>G	ENSP00000508742.2:n.*907T>G
ENST00000700021.1:c.1032T>G	ENSP00000514757.1:p.Ala344=
ENST00000700022.1:c.*416T>G	ENSP00000514758.1:n.*416T>G
ENST00000700023.1:n.2235T>G
ENST00000700024.1:n.2469T>G
ENST00000706954.1:c.1077T>G	ENSP00000516674.1:p.Ala359=
ENST00000706955.1:c.*1112T>G	ENSP00000516675.1:n.*1112T>G
ENST00000686459.1:c.*663T>G	ENSP00000508909.1:n.*663T>G
ENST00000688158.1:c.*1188T>G	ENSP00000509254.1:n.*1188T>G
ENST00000688308.1:c.1077T>G	ENSP00000508752.1:p.Ala359=
ENST00000688922.1:c.998T>G
ENST00000693560.1:c.1596T>G	ENSP00000509861.1:p.Ala532=
ENST00000371953.8:c.1077T>G MANE Select	ENSP00000361021.3:p.Ala359=
ENST00000371953.7:c.1077T>G	ENSP00000361021.3:p.Ala359=
NM_000314.5:c.1077T>G	NP_000305.3:p.Ala359=
NM_000314.6:c.1077T>G	NP_000305.3:p.Ala359=
NM_001304717.2:c.1596T>G	NP_001291646.2:p.Ala532=
NM_001304718.1:c.486T>G	NP_001291647.1:p.Ala162=
XM_006717926.2:c.1032T>G	XP_006717989.1:p.Ala344=
XM_011539982.1:c.981T>G	XP_011538284.1:p.Ala327=
XR_945791.1:n.1647T>G
NM_000314.7:c.1077T>G	NP_000305.3:p.Ala359=
NM_001304717.5:c.1596T>G	NP_001291646.4:p.Ala532=
NM_001304718.2:c.486T>G	NP_001291647.1:p.Ala162=
NM_000314.8:c.1077T>G MANE Select	NP_000305.3:p.Ala359=