Canonical Allele Identifier: CA377484980
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957963G>T , CM000672.2:g.87957963G>T GRCh38
NC_000010.10:g.89717720G>T , CM000672.1:g.89717720G>T GRCh37
NC_000010.9:g.89707700G>T NCBI36
NG_007466.2:g.99525G>T , LRG_311:g.99525G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.745G>T ENSP00000514759.2:p.Val249Leu
ENST00000710265.1:c.745G>T ENSP00000518161.1:p.Val249Leu
ENST00000472832.3:c.745G>T ENSP00000483066.2:p.Val249Leu
ENST00000688158.2:n.1480G>T
ENST00000688922.2:c.*575G>T ENSP00000508742.2:n.*575G>T
ENST00000700021.1:c.700G>T ENSP00000514757.1:p.Val234Leu
ENST00000700022.1:c.*84G>T ENSP00000514758.1:n.*84G>T
ENST00000700023.1:n.1903G>T
ENST00000700024.1:n.2137G>T
ENST00000700025.1:n.1514G>T
ENST00000700026.1:n.382G>T
ENST00000700029.1:c.579G>T
ENST00000706954.1:c.745G>T ENSP00000516674.1:p.Val249Leu
ENST00000706955.1:c.*780G>T ENSP00000516675.1:n.*780G>T
ENST00000686459.1:c.*331G>T ENSP00000508909.1:n.*331G>T
ENST00000688158.1:c.*856G>T ENSP00000509254.1:n.*856G>T
ENST00000688308.1:c.745G>T ENSP00000508752.1:p.Val249Leu
ENST00000688922.1:c.666G>T
ENST00000693560.1:c.1264G>T ENSP00000509861.1:p.Val422Leu
ENST00000371953.8:c.745G>T MANE Select ENSP00000361021.3:p.Val249Leu
ENST00000371953.7:c.745G>T ENSP00000361021.3:p.Val249Leu
ENST00000472832.2:c.172G>T ENSP00000483066.1:p.Val58Leu
NM_000314.5:c.745G>T NP_000305.3:p.Val249Leu
NM_000314.6:c.745G>T NP_000305.3:p.Val249Leu
NM_001304717.2:c.1264G>T NP_001291646.2:p.Val422Leu
NM_001304718.1:c.154G>T NP_001291647.1:p.Val52Leu
XM_006717926.2:c.700G>T XP_006717989.1:p.Val234Leu
XM_011539981.1:c.745G>T XP_011538283.1:p.Val249Leu
XM_011539982.1:c.649G>T XP_011538284.1:p.Val217Leu
XR_945791.1:n.1315G>T
NM_000314.7:c.745G>T NP_000305.3:p.Val249Leu
NM_001304717.5:c.1264G>T NP_001291646.4:p.Val422Leu
NM_001304718.2:c.154G>T NP_001291647.1:p.Val52Leu
NM_000314.8:c.745G>T MANE Select NP_000305.3:p.Val249Leu