Canonical Allele Identifier: CA377487168

Gene: PTEN

Linked Data

• dbSNP Id: rs2132289390
• MyVariant Identifiers: chr10:g.89725077C>G (hg19) ; chr10:g.87965320C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965320C>G , CM000672.2:g.87965320C>G	GRCh38
NC_000010.10:g.89725077C>G , CM000672.1:g.89725077C>G	GRCh37
NC_000010.9:g.89715057C>G	NCBI36
NG_007466.2:g.106882C>G , LRG_311:g.106882C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1153C>G	ENSP00000514759.2:p.Pro385Ala
ENST00000710265.1:c.*89C>G	ENSP00000518161.1:n.*89C>G
ENST00000688158.2:n.1795C>G
ENST00000688922.2:c.*890C>G	ENSP00000508742.2:n.*890C>G
ENST00000700021.1:c.1015C>G	ENSP00000514757.1:p.Pro339Ala
ENST00000700022.1:c.*399C>G	ENSP00000514758.1:n.*399C>G
ENST00000700023.1:n.2218C>G
ENST00000700024.1:n.2452C>G
ENST00000706954.1:c.1060C>G	ENSP00000516674.1:p.Pro354Ala
ENST00000706955.1:c.*1095C>G	ENSP00000516675.1:n.*1095C>G
ENST00000686459.1:c.*646C>G	ENSP00000508909.1:n.*646C>G
ENST00000688158.1:c.*1171C>G	ENSP00000509254.1:n.*1171C>G
ENST00000688308.1:c.1060C>G	ENSP00000508752.1:p.Pro354Ala
ENST00000688922.1:c.981C>G
ENST00000693560.1:c.1579C>G	ENSP00000509861.1:p.Pro527Ala
ENST00000371953.8:c.1060C>G MANE Select	ENSP00000361021.3:p.Pro354Ala
ENST00000371953.7:c.1060C>G	ENSP00000361021.3:p.Pro354Ala
NM_000314.5:c.1060C>G	NP_000305.3:p.Pro354Ala
NM_000314.6:c.1060C>G	NP_000305.3:p.Pro354Ala
NM_001304717.2:c.1579C>G	NP_001291646.2:p.Pro527Ala
NM_001304718.1:c.469C>G	NP_001291647.1:p.Pro157Ala
XM_006717926.2:c.1015C>G	XP_006717989.1:p.Pro339Ala
XM_011539982.1:c.964C>G	XP_011538284.1:p.Pro322Ala
XR_945791.1:n.1630C>G
NM_000314.7:c.1060C>G	NP_000305.3:p.Pro354Ala
NM_001304717.5:c.1579C>G	NP_001291646.4:p.Pro527Ala
NM_001304718.2:c.469C>G	NP_001291647.1:p.Pro157Ala
NM_000314.8:c.1060C>G MANE Select	NP_000305.3:p.Pro354Ala