Canonical Allele Identifier: CA470973894

Gene: PTEN

Linked Data

• dbSNP Id: rs2132281737
• MyVariant Identifiers: chr10:g.89720656A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960899A>G , CM000672.2:g.87960899A>G	GRCh38
NC_000010.10:g.89720656A>G , CM000672.1:g.89720656A>G	GRCh37
NC_000010.9:g.89710636A>G	NCBI36
NG_007466.2:g.102461A>G , LRG_311:g.102461A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.900A>G	ENSP00000514759.2:p.Lys300=
ENST00000710265.1:c.807A>G	ENSP00000518161.1:p.Lys269=
ENST00000472832.3:c.807A>G	ENSP00000483066.2:p.Lys269=
ENST00000688158.2:n.1542A>G
ENST00000688922.2:c.*637A>G	ENSP00000508742.2:n.*637A>G
ENST00000700021.1:c.762A>G	ENSP00000514757.1:p.Lys254=
ENST00000700022.1:c.*146A>G	ENSP00000514758.1:n.*146A>G
ENST00000700023.1:n.1965A>G
ENST00000700024.1:n.2199A>G
ENST00000700025.1:n.1576A>G
ENST00000700026.1:n.444A>G
ENST00000700029.1:c.734A>G
ENST00000706954.1:c.807A>G	ENSP00000516674.1:p.Lys269=
ENST00000706955.1:c.*842A>G	ENSP00000516675.1:n.*842A>G
ENST00000686459.1:c.*393A>G	ENSP00000508909.1:n.*393A>G
ENST00000688158.1:c.*918A>G	ENSP00000509254.1:n.*918A>G
ENST00000688308.1:c.807A>G	ENSP00000508752.1:p.Lys269=
ENST00000688922.1:c.728A>G
ENST00000693560.1:c.1326A>G	ENSP00000509861.1:p.Lys442=
ENST00000371953.8:c.807A>G MANE Select	ENSP00000361021.3:p.Lys269=
ENST00000371953.7:c.807A>G	ENSP00000361021.3:p.Lys269=
ENST00000472832.2:c.234A>G	ENSP00000483066.1:p.Lys78=
NM_000314.5:c.807A>G	NP_000305.3:p.Lys269=
NM_000314.6:c.807A>G	NP_000305.3:p.Lys269=
NM_001304717.2:c.1326A>G	NP_001291646.2:p.Lys442=
NM_001304718.1:c.216A>G	NP_001291647.1:p.Lys72=
XM_006717926.2:c.762A>G	XP_006717989.1:p.Lys254=
XM_011539981.1:c.807A>G	XP_011538283.1:p.Lys269=
XM_011539982.1:c.711A>G	XP_011538284.1:p.Lys237=
XR_945791.1:n.1377A>G
NM_000314.7:c.807A>G	NP_000305.3:p.Lys269=
NM_001304717.5:c.1326A>G	NP_001291646.4:p.Lys442=
NM_001304718.2:c.216A>G	NP_001291647.1:p.Lys72=
NM_000314.8:c.807A>G MANE Select	NP_000305.3:p.Lys269=