Canonical Allele Identifier: CA891839813
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954_87957956delinsGAT , CM000672.2:g.87957954_87957956delinsGAT GRCh38
NC_000010.10:g.89717711_89717713delinsGAT , CM000672.1:g.89717711_89717713delinsGAT GRCh37
NC_000010.9:g.89707691_89707693delinsGAT NCBI36
NG_007466.2:g.99516_99518delinsGAT , LRG_311:g.99516_99518delinsGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736_738delinsGAT ENSP00000514759.2:p.Pro246Asp
ENST00000710265.1:c.736_738delinsGAT ENSP00000518161.1:p.Pro246Asp
ENST00000472832.3:c.736_738delinsGAT ENSP00000483066.2:p.Pro246Asp
ENST00000688158.2:n.1471_1473delinsGAT
ENST00000688922.2:c.*566_*568delinsGAT ENSP00000508742.2:n.*566_*568delinsGAT
ENST00000700021.1:c.691_693delinsGAT ENSP00000514757.1:p.Pro231Asp
ENST00000700022.1:c.*75_*77delinsGAT ENSP00000514758.1:n.*75_*77delinsGAT
ENST00000700023.1:n.1894_1896delinsGAT
ENST00000700024.1:n.2128_2130delinsGAT
ENST00000700025.1:n.1505_1507delinsGAT
ENST00000700026.1:n.373_375delinsGAT
ENST00000700029.1:c.570_572delinsGAT
ENST00000706954.1:c.736_738delinsGAT ENSP00000516674.1:p.Pro246Asp
ENST00000706955.1:c.*771_*773delinsGAT ENSP00000516675.1:n.*771_*773delinsGAT
ENST00000686459.1:c.*322_*324delinsGAT ENSP00000508909.1:n.*322_*324delinsGAT
ENST00000688158.1:c.*847_*849delinsGAT ENSP00000509254.1:n.*847_*849delinsGAT
ENST00000688308.1:c.736_738delinsGAT ENSP00000508752.1:p.Pro246Asp
ENST00000688922.1:c.657_659delinsGAT
ENST00000693560.1:c.1255_1257delinsGAT ENSP00000509861.1:p.Pro419Asp
ENST00000371953.8:c.736_738delinsGAT MANE Select ENSP00000361021.3:p.Pro246Asp
ENST00000371953.7:c.736_738delinsGAT ENSP00000361021.3:p.Pro246Asp
ENST00000472832.2:c.163_165delinsGAT ENSP00000483066.1:p.Pro55Asp
NM_000314.5:c.736_738delinsGAT NP_000305.3:p.Pro246Asp
NM_000314.6:c.736_738delinsGAT NP_000305.3:p.Pro246Asp
NM_001304717.2:c.1255_1257delinsGAT NP_001291646.2:p.Pro419Asp
NM_001304718.1:c.145_147delinsGAT NP_001291647.1:p.Pro49Asp
XM_006717926.2:c.691_693delinsGAT XP_006717989.1:p.Pro231Asp
XM_011539981.1:c.736_738delinsGAT XP_011538283.1:p.Pro246Asp
XM_011539982.1:c.640_642delinsGAT XP_011538284.1:p.Pro214Asp
XR_945791.1:n.1306_1308delinsGAT
NM_000314.7:c.736_738delinsGAT NP_000305.3:p.Pro246Asp
NM_001304717.5:c.1255_1257delinsGAT NP_001291646.4:p.Pro419Asp
NM_001304718.2:c.145_147delinsGAT NP_001291647.1:p.Pro49Asp
NM_000314.8:c.736_738delinsGAT MANE Select NP_000305.3:p.Pro246Asp