Canonical Allele Identifier: CA377482087

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933035C>G , CM000672.2:g.87933035C>G	GRCh38
NC_000010.10:g.89692792C>G , CM000672.1:g.89692792C>G	GRCh37
NC_000010.9:g.89682772C>G	NCBI36
NG_007466.2:g.74597C>G , LRG_311:g.74597C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000314.8:c.276C>G MANE Select	NP_000305.3:p.Asp92Glu
ENST00000371953.8:c.276C>G MANE Select	ENSP00000361021.3:p.Asp92Glu
NM_000314.5:c.276C>G	NP_000305.3:p.Asp92Glu
NM_000314.6:c.276C>G	NP_000305.3:p.Asp92Glu
NM_000314.7:c.276C>G	NP_000305.3:p.Asp92Glu
NM_001304717.2:c.795C>G	NP_001291646.2:p.Asp265Glu
NM_001304717.5:c.795C>G	NP_001291646.4:p.Asp265Glu
NM_001304718.1:c.-475C>G	NP_001291647.1:n.-475C>G
NM_001304718.2:c.-475C>G	NP_001291647.1:n.-475C>G
ENST00000371953.7:c.276C>G	ENSP00000361021.3:p.Asp92Glu
ENST00000472832.3:c.276C>G	ENSP00000483066.2:p.Asp92Glu
ENST00000498703.1:n.102C>G
ENST00000610634.1:c.174C>G	ENSP00000477517.1:p.Asp58Glu
ENST00000686459.1:c.276C>G	ENSP00000508909.1:p.Asp92Glu
ENST00000688158.1:c.*387C>G	ENSP00000509254.1:n.*387C>G
ENST00000688158.2:n.1011C>G
ENST00000688308.1:c.276C>G	ENSP00000508752.1:p.Asp92Glu
ENST00000688922.1:c.197C>G
ENST00000688922.2:c.*106C>G	ENSP00000508742.2:n.*106C>G
ENST00000693560.1:c.795C>G	ENSP00000509861.1:p.Asp265Glu
ENST00000700021.1:c.231C>G	ENSP00000514757.1:p.Asp77Glu
ENST00000700022.1:c.276C>G	ENSP00000514758.1:p.Asp92Glu
ENST00000700029.1:c.110C>G
ENST00000700029.2:c.276C>G	ENSP00000514759.2:p.Asp92Glu
ENST00000706954.1:c.276C>G	ENSP00000516674.1:p.Asp92Glu
ENST00000706955.1:c.*311C>G	ENSP00000516675.1:n.*311C>G
ENST00000710265.1:c.276C>G	ENSP00000518161.1:p.Asp92Glu
XM_006717926.2:c.231C>G	XP_006717989.1:p.Asp77Glu
XM_011539981.1:c.276C>G	XP_011538283.1:p.Asp92Glu
XM_011539982.1:c.180C>G	XP_011538284.1:p.Asp60Glu
XR_945789.1:n.988C>G
XR_945790.1:n.988C>G
XR_945791.1:n.988C>G