Canonical Allele Identifier: CA470670056
Gene: PTEN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89717770A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958013A>T , CM000672.2:g.87958013A>T GRCh38
NC_000010.10:g.89717770A>T , CM000672.1:g.89717770A>T GRCh37
NC_000010.9:g.89707750A>T NCBI36
NG_007466.2:g.99575A>T , LRG_311:g.99575A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.795A>T ENSP00000514759.2:p.Leu265=
ENST00000710265.1:c.795A>T ENSP00000518161.1:p.Leu265=
ENST00000472832.3:c.795A>T ENSP00000483066.2:p.Leu265=
ENST00000688158.2:n.1530A>T
ENST00000688922.2:c.*625A>T ENSP00000508742.2:n.*625A>T
ENST00000700021.1:c.750A>T ENSP00000514757.1:p.Leu250=
ENST00000700022.1:c.*134A>T ENSP00000514758.1:n.*134A>T
ENST00000700023.1:n.1953A>T
ENST00000700024.1:n.2187A>T
ENST00000700025.1:n.1564A>T
ENST00000700026.1:n.432A>T
ENST00000700029.1:c.629A>T
ENST00000706954.1:c.795A>T ENSP00000516674.1:p.Leu265=
ENST00000706955.1:c.*830A>T ENSP00000516675.1:n.*830A>T
ENST00000686459.1:c.*381A>T ENSP00000508909.1:n.*381A>T
ENST00000688158.1:c.*906A>T ENSP00000509254.1:n.*906A>T
ENST00000688308.1:c.795A>T ENSP00000508752.1:p.Leu265=
ENST00000688922.1:c.716A>T
ENST00000693560.1:c.1314A>T ENSP00000509861.1:p.Leu438=
ENST00000371953.8:c.795A>T MANE Select ENSP00000361021.3:p.Leu265=
ENST00000371953.7:c.795A>T ENSP00000361021.3:p.Leu265=
ENST00000472832.2:c.222A>T ENSP00000483066.1:p.Leu74=
NM_000314.5:c.795A>T NP_000305.3:p.Leu265=
NM_000314.6:c.795A>T NP_000305.3:p.Leu265=
NM_001304717.2:c.1314A>T NP_001291646.2:p.Leu438=
NM_001304718.1:c.204A>T NP_001291647.1:p.Leu68=
XM_006717926.2:c.750A>T XP_006717989.1:p.Leu250=
XM_011539981.1:c.795A>T XP_011538283.1:p.Leu265=
XM_011539982.1:c.699A>T XP_011538284.1:p.Leu233=
XR_945791.1:n.1365A>T
NM_000314.7:c.795A>T NP_000305.3:p.Leu265=
NM_001304717.5:c.1314A>T NP_001291646.4:p.Leu438=
NM_001304718.2:c.204A>T NP_001291647.1:p.Leu68=
NM_000314.8:c.795A>T MANE Select NP_000305.3:p.Leu265=