Canonical Allele Identifier: CA470670908

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725070A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965313A>T , CM000672.2:g.87965313A>T	GRCh38
NC_000010.10:g.89725070A>T , CM000672.1:g.89725070A>T	GRCh37
NC_000010.9:g.89715050A>T	NCBI36
NG_007466.2:g.106875A>T , LRG_311:g.106875A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1146A>T	ENSP00000514759.2:p.Val382=
ENST00000710265.1:c.*82A>T	ENSP00000518161.1:n.*82A>T
ENST00000688158.2:n.1788A>T
ENST00000688922.2:c.*883A>T	ENSP00000508742.2:n.*883A>T
ENST00000700021.1:c.1008A>T	ENSP00000514757.1:p.Val336=
ENST00000700022.1:c.*392A>T	ENSP00000514758.1:n.*392A>T
ENST00000700023.1:n.2211A>T
ENST00000700024.1:n.2445A>T
ENST00000706954.1:c.1053A>T	ENSP00000516674.1:p.Val351=
ENST00000706955.1:c.*1088A>T	ENSP00000516675.1:n.*1088A>T
ENST00000686459.1:c.*639A>T	ENSP00000508909.1:n.*639A>T
ENST00000688158.1:c.*1164A>T	ENSP00000509254.1:n.*1164A>T
ENST00000688308.1:c.1053A>T	ENSP00000508752.1:p.Val351=
ENST00000688922.1:c.974A>T
ENST00000693560.1:c.1572A>T	ENSP00000509861.1:p.Val524=
ENST00000371953.8:c.1053A>T MANE Select	ENSP00000361021.3:p.Val351=
ENST00000371953.7:c.1053A>T	ENSP00000361021.3:p.Val351=
NM_000314.5:c.1053A>T	NP_000305.3:p.Val351=
NM_000314.6:c.1053A>T	NP_000305.3:p.Val351=
NM_001304717.2:c.1572A>T	NP_001291646.2:p.Val524=
NM_001304718.1:c.462A>T	NP_001291647.1:p.Val154=
XM_006717926.2:c.1008A>T	XP_006717989.1:p.Val336=
XM_011539982.1:c.957A>T	XP_011538284.1:p.Val319=
XR_945791.1:n.1623A>T
NM_000314.7:c.1053A>T	NP_000305.3:p.Val351=
NM_001304717.5:c.1572A>T	NP_001291646.4:p.Val524=
NM_001304718.2:c.462A>T	NP_001291647.1:p.Val154=
NM_000314.8:c.1053A>T MANE Select	NP_000305.3:p.Val351=