Canonical Allele Identifier: CA470667784

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952249C>G , CM000672.2:g.87952249C>G	GRCh38
NC_000010.10:g.89712006C>G , CM000672.1:g.89712006C>G	GRCh37
NC_000010.9:g.89701986C>G	NCBI36
NG_007466.2:g.93811C>G , LRG_311:g.93811C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.624C>G MANE Select	NP_000305.3:p.Gly208=
ENST00000371953.8:c.624C>G MANE Select	ENSP00000361021.3:p.Gly208=
NM_000314.5:c.624C>G	NP_000305.3:p.Gly208=
NM_000314.6:c.624C>G	NP_000305.3:p.Gly208=
NM_000314.7:c.624C>G	NP_000305.3:p.Gly208=
NM_001304717.2:c.1143C>G	NP_001291646.2:p.Gly381=
NM_001304717.5:c.1143C>G	NP_001291646.4:p.Gly381=
NM_001304718.1:c.33C>G	NP_001291647.1:p.Gly11=
NM_001304718.2:c.33C>G	NP_001291647.1:p.Gly11=
ENST00000371953.7:c.624C>G	ENSP00000361021.3:p.Gly208=
ENST00000472832.2:c.51C>G	ENSP00000483066.1:p.Gly17=
ENST00000472832.3:c.624C>G	ENSP00000483066.2:p.Gly208=
ENST00000686459.1:c.*210C>G	ENSP00000508909.1:n.*210C>G
ENST00000688158.1:c.*735C>G	ENSP00000509254.1:n.*735C>G
ENST00000688158.2:n.1359C>G
ENST00000688308.1:c.624C>G	ENSP00000508752.1:p.Gly208=
ENST00000688922.1:c.545C>G
ENST00000688922.2:c.*454C>G	ENSP00000508742.2:n.*454C>G
ENST00000693560.1:c.1143C>G	ENSP00000509861.1:p.Gly381=
ENST00000700021.1:c.579C>G	ENSP00000514757.1:p.Gly193=
ENST00000700022.1:c.493-5604C>G	ENSP00000514758.1:n.493-5604C>G
ENST00000700023.1:n.1782C>G
ENST00000700024.1:n.2016C>G
ENST00000700025.1:n.1393C>G
ENST00000700029.1:c.458C>G
ENST00000700029.2:c.624C>G	ENSP00000514759.2:p.Gly208=
ENST00000706954.1:c.624C>G	ENSP00000516674.1:p.Gly208=
ENST00000706955.1:c.*659C>G	ENSP00000516675.1:n.*659C>G
ENST00000710265.1:c.624C>G	ENSP00000518161.1:p.Gly208=
XM_006717926.2:c.579C>G	XP_006717989.1:p.Gly193=
XM_011539981.1:c.624C>G	XP_011538283.1:p.Gly208=
XM_011539982.1:c.528C>G	XP_011538284.1:p.Gly176=
XR_945791.1:n.1205-5604C>G