Canonical Allele Identifier: CA891839794
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957949_87957950delinsAA , CM000672.2:g.87957949_87957950delinsAA GRCh38
NC_000010.10:g.89717706_89717707delinsAA , CM000672.1:g.89717706_89717707delinsAA GRCh37
NC_000010.9:g.89707686_89707687delinsAA NCBI36
NG_007466.2:g.99511_99512delinsAA , LRG_311:g.99511_99512delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.731_732delinsAA ENSP00000514759.2:p.Pro244Gln
ENST00000710265.1:c.731_732delinsAA ENSP00000518161.1:p.Pro244Gln
ENST00000472832.3:c.731_732delinsAA ENSP00000483066.2:p.Pro244Gln
ENST00000688158.2:n.1466_1467delinsAA
ENST00000688922.2:c.*561_*562delinsAA ENSP00000508742.2:n.*561_*562delinsAA
ENST00000700021.1:c.686_687delinsAA ENSP00000514757.1:p.Pro229Gln
ENST00000700022.1:c.*70_*71delinsAA ENSP00000514758.1:n.*70_*71delinsAA
ENST00000700023.1:n.1889_1890delinsAA
ENST00000700024.1:n.2123_2124delinsAA
ENST00000700025.1:n.1500_1501delinsAA
ENST00000700026.1:n.368_369delinsAA
ENST00000700029.1:c.565_566delinsAA
ENST00000706954.1:c.731_732delinsAA ENSP00000516674.1:p.Pro244Gln
ENST00000706955.1:c.*766_*767delinsAA ENSP00000516675.1:n.*766_*767delinsAA
ENST00000686459.1:c.*317_*318delinsAA ENSP00000508909.1:n.*317_*318delinsAA
ENST00000688158.1:c.*842_*843delinsAA ENSP00000509254.1:n.*842_*843delinsAA
ENST00000688308.1:c.731_732delinsAA ENSP00000508752.1:p.Pro244Gln
ENST00000688922.1:c.652_653delinsAA
ENST00000693560.1:c.1250_1251delinsAA ENSP00000509861.1:p.Pro417Gln
ENST00000371953.8:c.731_732delinsAA MANE Select ENSP00000361021.3:p.Pro244Gln
ENST00000371953.7:c.731_732delinsAA ENSP00000361021.3:p.Pro244Gln
ENST00000472832.2:c.158_159delinsAA ENSP00000483066.1:p.Pro53Gln
NM_000314.5:c.731_732delinsAA NP_000305.3:p.Pro244Gln
NM_000314.6:c.731_732delinsAA NP_000305.3:p.Pro244Gln
NM_001304717.2:c.1250_1251delinsAA NP_001291646.2:p.Pro417Gln
NM_001304718.1:c.140_141delinsAA NP_001291647.1:p.Pro47Gln
XM_006717926.2:c.686_687delinsAA XP_006717989.1:p.Pro229Gln
XM_011539981.1:c.731_732delinsAA XP_011538283.1:p.Pro244Gln
XM_011539982.1:c.635_636delinsAA XP_011538284.1:p.Pro212Gln
XR_945791.1:n.1301_1302delinsAA
NM_000314.7:c.731_732delinsAA NP_000305.3:p.Pro244Gln
NM_001304717.5:c.1250_1251delinsAA NP_001291646.4:p.Pro417Gln
NM_001304718.2:c.140_141delinsAA NP_001291647.1:p.Pro47Gln
NM_000314.8:c.731_732delinsAA MANE Select NP_000305.3:p.Pro244Gln