Canonical Allele Identifier: CA377487414

Gene: PTEN

Linked Data

• dbSNP Id: rs1554826059
• MyVariant Identifiers: chr10:g.89725189C>G (hg19) ; chr10:g.87965432C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965432C>G , CM000672.2:g.87965432C>G	GRCh38
NC_000010.10:g.89725189C>G , CM000672.1:g.89725189C>G	GRCh37
NC_000010.9:g.89715169C>G	NCBI36
NG_007466.2:g.106994C>G , LRG_311:g.106994C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1265C>G	ENSP00000514759.2:p.Pro422Arg
ENST00000710265.1:c.*201C>G	ENSP00000518161.1:n.*201C>G
ENST00000688158.2:n.1907C>G
ENST00000688922.2:c.*1002C>G	ENSP00000508742.2:n.*1002C>G
ENST00000700021.1:c.1127C>G	ENSP00000514757.1:p.Pro376Arg
ENST00000700022.1:c.*511C>G	ENSP00000514758.1:n.*511C>G
ENST00000700023.1:n.2330C>G
ENST00000700024.1:n.2564C>G
ENST00000706954.1:c.1172C>G	ENSP00000516674.1:p.Pro391Arg
ENST00000706955.1:c.*1207C>G	ENSP00000516675.1:n.*1207C>G
ENST00000686459.1:c.*758C>G	ENSP00000508909.1:n.*758C>G
ENST00000688158.1:c.*1283C>G	ENSP00000509254.1:n.*1283C>G
ENST00000688308.1:c.1172C>G	ENSP00000508752.1:p.Pro391Arg
ENST00000688922.1:c.1093C>G
ENST00000693560.1:c.1691C>G	ENSP00000509861.1:p.Pro564Arg
ENST00000371953.8:c.1172C>G MANE Select	ENSP00000361021.3:p.Pro391Arg
ENST00000371953.7:c.1172C>G	ENSP00000361021.3:p.Pro391Arg
NM_000314.5:c.1172C>G	NP_000305.3:p.Pro391Arg
NM_000314.6:c.1172C>G	NP_000305.3:p.Pro391Arg
NM_001304717.2:c.1691C>G	NP_001291646.2:p.Pro564Arg
NM_001304718.1:c.581C>G	NP_001291647.1:p.Pro194Arg
XM_006717926.2:c.1127C>G	XP_006717989.1:p.Pro376Arg
XM_011539982.1:c.1076C>G	XP_011538284.1:p.Pro359Arg
XR_945791.1:n.1742C>G
NM_000314.7:c.1172C>G	NP_000305.3:p.Pro391Arg
NM_001304717.5:c.1691C>G	NP_001291646.4:p.Pro564Arg
NM_001304718.2:c.581C>G	NP_001291647.1:p.Pro194Arg
NM_000314.8:c.1172C>G MANE Select	NP_000305.3:p.Pro391Arg