Canonical Allele Identifier: CA891839823
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954_87957956delinsGTT , CM000672.2:g.87957954_87957956delinsGTT GRCh38
NC_000010.10:g.89717711_89717713delinsGTT , CM000672.1:g.89717711_89717713delinsGTT GRCh37
NC_000010.9:g.89707691_89707693delinsGTT NCBI36
NG_007466.2:g.99516_99518delinsGTT , LRG_311:g.99516_99518delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736_738delinsGTT ENSP00000514759.2:p.Pro246Val
ENST00000710265.1:c.736_738delinsGTT ENSP00000518161.1:p.Pro246Val
ENST00000472832.3:c.736_738delinsGTT ENSP00000483066.2:p.Pro246Val
ENST00000688158.2:n.1471_1473delinsGTT
ENST00000688922.2:c.*566_*568delinsGTT ENSP00000508742.2:n.*566_*568delinsGTT
ENST00000700021.1:c.691_693delinsGTT ENSP00000514757.1:p.Pro231Val
ENST00000700022.1:c.*75_*77delinsGTT ENSP00000514758.1:n.*75_*77delinsGTT
ENST00000700023.1:n.1894_1896delinsGTT
ENST00000700024.1:n.2128_2130delinsGTT
ENST00000700025.1:n.1505_1507delinsGTT
ENST00000700026.1:n.373_375delinsGTT
ENST00000700029.1:c.570_572delinsGTT
ENST00000706954.1:c.736_738delinsGTT ENSP00000516674.1:p.Pro246Val
ENST00000706955.1:c.*771_*773delinsGTT ENSP00000516675.1:n.*771_*773delinsGTT
ENST00000686459.1:c.*322_*324delinsGTT ENSP00000508909.1:n.*322_*324delinsGTT
ENST00000688158.1:c.*847_*849delinsGTT ENSP00000509254.1:n.*847_*849delinsGTT
ENST00000688308.1:c.736_738delinsGTT ENSP00000508752.1:p.Pro246Val
ENST00000688922.1:c.657_659delinsGTT
ENST00000693560.1:c.1255_1257delinsGTT ENSP00000509861.1:p.Pro419Val
ENST00000371953.8:c.736_738delinsGTT MANE Select ENSP00000361021.3:p.Pro246Val
ENST00000371953.7:c.736_738delinsGTT ENSP00000361021.3:p.Pro246Val
ENST00000472832.2:c.163_165delinsGTT ENSP00000483066.1:p.Pro55Val
NM_000314.5:c.736_738delinsGTT NP_000305.3:p.Pro246Val
NM_000314.6:c.736_738delinsGTT NP_000305.3:p.Pro246Val
NM_001304717.2:c.1255_1257delinsGTT NP_001291646.2:p.Pro419Val
NM_001304718.1:c.145_147delinsGTT NP_001291647.1:p.Pro49Val
XM_006717926.2:c.691_693delinsGTT XP_006717989.1:p.Pro231Val
XM_011539981.1:c.736_738delinsGTT XP_011538283.1:p.Pro246Val
XM_011539982.1:c.640_642delinsGTT XP_011538284.1:p.Pro214Val
XR_945791.1:n.1306_1308delinsGTT
NM_000314.7:c.736_738delinsGTT NP_000305.3:p.Pro246Val
NM_001304717.5:c.1255_1257delinsGTT NP_001291646.4:p.Pro419Val
NM_001304718.2:c.145_147delinsGTT NP_001291647.1:p.Pro49Val
NM_000314.8:c.736_738delinsGTT MANE Select NP_000305.3:p.Pro246Val