Canonical Allele Identifier: CA377487150

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725069T>G (hg19) ; chr10:g.87965312T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965312T>G , CM000672.2:g.87965312T>G	GRCh38
NC_000010.10:g.89725069T>G , CM000672.1:g.89725069T>G	GRCh37
NC_000010.9:g.89715049T>G	NCBI36
NG_007466.2:g.106874T>G , LRG_311:g.106874T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1145T>G	ENSP00000514759.2:p.Val382Gly
ENST00000710265.1:c.*81T>G	ENSP00000518161.1:n.*81T>G
ENST00000688158.2:n.1787T>G
ENST00000688922.2:c.*882T>G	ENSP00000508742.2:n.*882T>G
ENST00000700021.1:c.1007T>G	ENSP00000514757.1:p.Val336Gly
ENST00000700022.1:c.*391T>G	ENSP00000514758.1:n.*391T>G
ENST00000700023.1:n.2210T>G
ENST00000700024.1:n.2444T>G
ENST00000706954.1:c.1052T>G	ENSP00000516674.1:p.Val351Gly
ENST00000706955.1:c.*1087T>G	ENSP00000516675.1:n.*1087T>G
ENST00000686459.1:c.*638T>G	ENSP00000508909.1:n.*638T>G
ENST00000688158.1:c.*1163T>G	ENSP00000509254.1:n.*1163T>G
ENST00000688308.1:c.1052T>G	ENSP00000508752.1:p.Val351Gly
ENST00000688922.1:c.973T>G
ENST00000693560.1:c.1571T>G	ENSP00000509861.1:p.Val524Gly
ENST00000371953.8:c.1052T>G MANE Select	ENSP00000361021.3:p.Val351Gly
ENST00000371953.7:c.1052T>G	ENSP00000361021.3:p.Val351Gly
NM_000314.5:c.1052T>G	NP_000305.3:p.Val351Gly
NM_000314.6:c.1052T>G	NP_000305.3:p.Val351Gly
NM_001304717.2:c.1571T>G	NP_001291646.2:p.Val524Gly
NM_001304718.1:c.461T>G	NP_001291647.1:p.Val154Gly
XM_006717926.2:c.1007T>G	XP_006717989.1:p.Val336Gly
XM_011539982.1:c.956T>G	XP_011538284.1:p.Val319Gly
XR_945791.1:n.1622T>G
NM_000314.7:c.1052T>G	NP_000305.3:p.Val351Gly
NM_001304717.5:c.1571T>G	NP_001291646.4:p.Val524Gly
NM_001304718.2:c.461T>G	NP_001291647.1:p.Val154Gly
NM_000314.8:c.1052T>G MANE Select	NP_000305.3:p.Val351Gly