Canonical Allele Identifier: CA377487421

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725192T>A (hg19) ; chr10:g.87965435T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965435T>A , CM000672.2:g.87965435T>A	GRCh38
NC_000010.10:g.89725192T>A , CM000672.1:g.89725192T>A	GRCh37
NC_000010.9:g.89715172T>A	NCBI36
NG_007466.2:g.106997T>A , LRG_311:g.106997T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1268T>A	ENSP00000514759.2:p.Phe423Tyr
ENST00000710265.1:c.*204T>A	ENSP00000518161.1:n.*204T>A
ENST00000688158.2:n.1910T>A
ENST00000688922.2:c.*1005T>A	ENSP00000508742.2:n.*1005T>A
ENST00000700021.1:c.1130T>A	ENSP00000514757.1:p.Phe377Tyr
ENST00000700022.1:c.*514T>A	ENSP00000514758.1:n.*514T>A
ENST00000700023.1:n.2333T>A
ENST00000700024.1:n.2567T>A
ENST00000706954.1:c.1175T>A	ENSP00000516674.1:p.Phe392Tyr
ENST00000706955.1:c.*1210T>A	ENSP00000516675.1:n.*1210T>A
ENST00000686459.1:c.*761T>A	ENSP00000508909.1:n.*761T>A
ENST00000688158.1:c.*1286T>A	ENSP00000509254.1:n.*1286T>A
ENST00000688308.1:c.1175T>A	ENSP00000508752.1:p.Phe392Tyr
ENST00000688922.1:c.1096T>A
ENST00000693560.1:c.1694T>A	ENSP00000509861.1:p.Phe565Tyr
ENST00000371953.8:c.1175T>A MANE Select	ENSP00000361021.3:p.Phe392Tyr
ENST00000371953.7:c.1175T>A	ENSP00000361021.3:p.Phe392Tyr
NM_000314.5:c.1175T>A	NP_000305.3:p.Phe392Tyr
NM_000314.6:c.1175T>A	NP_000305.3:p.Phe392Tyr
NM_001304717.2:c.1694T>A	NP_001291646.2:p.Phe565Tyr
NM_001304718.1:c.584T>A	NP_001291647.1:p.Phe195Tyr
XM_006717926.2:c.1130T>A	XP_006717989.1:p.Phe377Tyr
XM_011539982.1:c.1079T>A	XP_011538284.1:p.Phe360Tyr
XR_945791.1:n.1745T>A
NM_000314.7:c.1175T>A	NP_000305.3:p.Phe392Tyr
NM_001304717.5:c.1694T>A	NP_001291646.4:p.Phe565Tyr
NM_001304718.2:c.584T>A	NP_001291647.1:p.Phe195Tyr
NM_000314.8:c.1175T>A MANE Select	NP_000305.3:p.Phe392Tyr