Canonical Allele Identifier: CA377487241

Gene: PTEN

Linked Data

• dbSNP Id: rs2132289674
• MyVariant Identifiers: chr10:g.89725116C>G (hg19) ; chr10:g.87965359C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965359C>G , CM000672.2:g.87965359C>G	GRCh38
NC_000010.10:g.89725116C>G , CM000672.1:g.89725116C>G	GRCh37
NC_000010.9:g.89715096C>G	NCBI36
NG_007466.2:g.106921C>G , LRG_311:g.106921C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1192C>G	ENSP00000514759.2:p.Pro398Ala
ENST00000710265.1:c.*128C>G	ENSP00000518161.1:n.*128C>G
ENST00000688158.2:n.1834C>G
ENST00000688922.2:c.*929C>G	ENSP00000508742.2:n.*929C>G
ENST00000700021.1:c.1054C>G	ENSP00000514757.1:p.Pro352Ala
ENST00000700022.1:c.*438C>G	ENSP00000514758.1:n.*438C>G
ENST00000700023.1:n.2257C>G
ENST00000700024.1:n.2491C>G
ENST00000706954.1:c.1099C>G	ENSP00000516674.1:p.Pro367Ala
ENST00000706955.1:c.*1134C>G	ENSP00000516675.1:n.*1134C>G
ENST00000686459.1:c.*685C>G	ENSP00000508909.1:n.*685C>G
ENST00000688158.1:c.*1210C>G	ENSP00000509254.1:n.*1210C>G
ENST00000688308.1:c.1099C>G	ENSP00000508752.1:p.Pro367Ala
ENST00000688922.1:c.1020C>G
ENST00000693560.1:c.1618C>G	ENSP00000509861.1:p.Pro540Ala
ENST00000371953.8:c.1099C>G MANE Select	ENSP00000361021.3:p.Pro367Ala
ENST00000371953.7:c.1099C>G	ENSP00000361021.3:p.Pro367Ala
NM_000314.5:c.1099C>G	NP_000305.3:p.Pro367Ala
NM_000314.6:c.1099C>G	NP_000305.3:p.Pro367Ala
NM_001304717.2:c.1618C>G	NP_001291646.2:p.Pro540Ala
NM_001304718.1:c.508C>G	NP_001291647.1:p.Pro170Ala
XM_006717926.2:c.1054C>G	XP_006717989.1:p.Pro352Ala
XM_011539982.1:c.1003C>G	XP_011538284.1:p.Pro335Ala
XR_945791.1:n.1669C>G
NM_000314.7:c.1099C>G	NP_000305.3:p.Pro367Ala
NM_001304717.5:c.1618C>G	NP_001291646.4:p.Pro540Ala
NM_001304718.2:c.508C>G	NP_001291647.1:p.Pro170Ala
NM_000314.8:c.1099C>G MANE Select	NP_000305.3:p.Pro367Ala