Canonical Allele Identifier: CA377487293

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725138C>G (hg19) ; chr10:g.87965381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965381C>G , CM000672.2:g.87965381C>G	GRCh38
NC_000010.10:g.89725138C>G , CM000672.1:g.89725138C>G	GRCh37
NC_000010.9:g.89715118C>G	NCBI36
NG_007466.2:g.106943C>G , LRG_311:g.106943C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1214C>G	ENSP00000514759.2:p.Pro405Arg
ENST00000710265.1:c.*150C>G	ENSP00000518161.1:n.*150C>G
ENST00000688158.2:n.1856C>G
ENST00000688922.2:c.*951C>G	ENSP00000508742.2:n.*951C>G
ENST00000700021.1:c.1076C>G	ENSP00000514757.1:p.Pro359Arg
ENST00000700022.1:c.*460C>G	ENSP00000514758.1:n.*460C>G
ENST00000700023.1:n.2279C>G
ENST00000700024.1:n.2513C>G
ENST00000706954.1:c.1121C>G	ENSP00000516674.1:p.Pro374Arg
ENST00000706955.1:c.*1156C>G	ENSP00000516675.1:n.*1156C>G
ENST00000686459.1:c.*707C>G	ENSP00000508909.1:n.*707C>G
ENST00000688158.1:c.*1232C>G	ENSP00000509254.1:n.*1232C>G
ENST00000688308.1:c.1121C>G	ENSP00000508752.1:p.Pro374Arg
ENST00000688922.1:c.1042C>G
ENST00000693560.1:c.1640C>G	ENSP00000509861.1:p.Pro547Arg
ENST00000371953.8:c.1121C>G MANE Select	ENSP00000361021.3:p.Pro374Arg
ENST00000371953.7:c.1121C>G	ENSP00000361021.3:p.Pro374Arg
NM_000314.5:c.1121C>G	NP_000305.3:p.Pro374Arg
NM_000314.6:c.1121C>G	NP_000305.3:p.Pro374Arg
NM_001304717.2:c.1640C>G	NP_001291646.2:p.Pro547Arg
NM_001304718.1:c.530C>G	NP_001291647.1:p.Pro177Arg
XM_006717926.2:c.1076C>G	XP_006717989.1:p.Pro359Arg
XM_011539982.1:c.1025C>G	XP_011538284.1:p.Pro342Arg
XR_945791.1:n.1691C>G
NM_000314.7:c.1121C>G	NP_000305.3:p.Pro374Arg
NM_001304717.5:c.1640C>G	NP_001291646.4:p.Pro547Arg
NM_001304718.2:c.530C>G	NP_001291647.1:p.Pro177Arg
NM_000314.8:c.1121C>G MANE Select	NP_000305.3:p.Pro374Arg