Canonical Allele Identifier: CA891836746
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961066_87961067delinsCA , CM000672.2:g.87961066_87961067delinsCA GRCh38
NC_000010.10:g.89720823_89720824delinsCA , CM000672.1:g.89720823_89720824delinsCA GRCh37
NC_000010.9:g.89710803_89710804delinsCA NCBI36
NG_007466.2:g.102628_102629delinsCA , LRG_311:g.102628_102629delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1067_1068delinsCA ENSP00000514759.2:p.Leu356Pro
ENST00000710265.1:c.974_975delinsCA ENSP00000518161.1:p.Leu325Pro
ENST00000472832.3:c.974_975delinsCA ENSP00000483066.2:p.Leu325Pro
ENST00000688158.2:n.1709_1710delinsCA
ENST00000688922.2:c.*804_*805delinsCA ENSP00000508742.2:n.*804_*805delinsCA
ENST00000700021.1:c.929_930delinsCA ENSP00000514757.1:p.Leu310Pro
ENST00000700022.1:c.*313_*314delinsCA ENSP00000514758.1:n.*313_*314delinsCA
ENST00000700023.1:n.2132_2133delinsCA
ENST00000700024.1:n.2366_2367delinsCA
ENST00000700025.1:n.1743_1744delinsCA
ENST00000700026.1:n.611_612delinsCA
ENST00000706954.1:c.974_975delinsCA ENSP00000516674.1:p.Leu325Pro
ENST00000706955.1:c.*1009_*1010delinsCA ENSP00000516675.1:n.*1009_*1010delinsCA
ENST00000686459.1:c.*560_*561delinsCA ENSP00000508909.1:n.*560_*561delinsCA
ENST00000688158.1:c.*1085_*1086delinsCA ENSP00000509254.1:n.*1085_*1086delinsCA
ENST00000688308.1:c.974_975delinsCA ENSP00000508752.1:p.Leu325Pro
ENST00000688922.1:c.895_896delinsCA
ENST00000693560.1:c.1493_1494delinsCA ENSP00000509861.1:p.Leu498Pro
ENST00000371953.8:c.974_975delinsCA MANE Select ENSP00000361021.3:p.Leu325Pro
ENST00000371953.7:c.974_975delinsCA ENSP00000361021.3:p.Leu325Pro
ENST00000472832.2:c.401_402delinsCA ENSP00000483066.1:p.Leu134Pro
NM_000314.5:c.974_975delinsCA NP_000305.3:p.Leu325Pro
NM_000314.6:c.974_975delinsCA NP_000305.3:p.Leu325Pro
NM_001304717.2:c.1493_1494delinsCA NP_001291646.2:p.Leu498Pro
NM_001304718.1:c.383_384delinsCA NP_001291647.1:p.Leu128Pro
XM_006717926.2:c.929_930delinsCA XP_006717989.1:p.Leu310Pro
XM_011539981.1:c.974_975delinsCA XP_011538283.1:p.Leu325Pro
XM_011539982.1:c.878_879delinsCA XP_011538284.1:p.Leu293Pro
XR_945791.1:n.1544_1545delinsCA
NM_000314.7:c.974_975delinsCA NP_000305.3:p.Leu325Pro
NM_001304717.5:c.1493_1494delinsCA NP_001291646.4:p.Leu498Pro
NM_001304718.2:c.383_384delinsCA NP_001291647.1:p.Leu128Pro
NM_000314.8:c.974_975delinsCA MANE Select NP_000305.3:p.Leu325Pro