Canonical Allele Identifier: CA891839830
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957955_87957956delinsAT , CM000672.2:g.87957955_87957956delinsAT GRCh38
NC_000010.10:g.89717712_89717713delinsAT , CM000672.1:g.89717712_89717713delinsAT GRCh37
NC_000010.9:g.89707692_89707693delinsAT NCBI36
NG_007466.2:g.99517_99518delinsAT , LRG_311:g.99517_99518delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.737_738delinsAT ENSP00000514759.2:p.Pro246His
ENST00000710265.1:c.737_738delinsAT ENSP00000518161.1:p.Pro246His
ENST00000472832.3:c.737_738delinsAT ENSP00000483066.2:p.Pro246His
ENST00000688158.2:n.1472_1473delinsAT
ENST00000688922.2:c.*567_*568delinsAT ENSP00000508742.2:n.*567_*568delinsAT
ENST00000700021.1:c.692_693delinsAT ENSP00000514757.1:p.Pro231His
ENST00000700022.1:c.*76_*77delinsAT ENSP00000514758.1:n.*76_*77delinsAT
ENST00000700023.1:n.1895_1896delinsAT
ENST00000700024.1:n.2129_2130delinsAT
ENST00000700025.1:n.1506_1507delinsAT
ENST00000700026.1:n.374_375delinsAT
ENST00000700029.1:c.571_572delinsAT
ENST00000706954.1:c.737_738delinsAT ENSP00000516674.1:p.Pro246His
ENST00000706955.1:c.*772_*773delinsAT ENSP00000516675.1:n.*772_*773delinsAT
ENST00000686459.1:c.*323_*324delinsAT ENSP00000508909.1:n.*323_*324delinsAT
ENST00000688158.1:c.*848_*849delinsAT ENSP00000509254.1:n.*848_*849delinsAT
ENST00000688308.1:c.737_738delinsAT ENSP00000508752.1:p.Pro246His
ENST00000688922.1:c.658_659delinsAT
ENST00000693560.1:c.1256_1257delinsAT ENSP00000509861.1:p.Pro419His
ENST00000371953.8:c.737_738delinsAT MANE Select ENSP00000361021.3:p.Pro246His
ENST00000371953.7:c.737_738delinsAT ENSP00000361021.3:p.Pro246His
ENST00000472832.2:c.164_165delinsAT ENSP00000483066.1:p.Pro55His
NM_000314.5:c.737_738delinsAT NP_000305.3:p.Pro246His
NM_000314.6:c.737_738delinsAT NP_000305.3:p.Pro246His
NM_001304717.2:c.1256_1257delinsAT NP_001291646.2:p.Pro419His
NM_001304718.1:c.146_147delinsAT NP_001291647.1:p.Pro49His
XM_006717926.2:c.692_693delinsAT XP_006717989.1:p.Pro231His
XM_011539981.1:c.737_738delinsAT XP_011538283.1:p.Pro246His
XM_011539982.1:c.641_642delinsAT XP_011538284.1:p.Pro214His
XR_945791.1:n.1307_1308delinsAT
NM_000314.7:c.737_738delinsAT NP_000305.3:p.Pro246His
NM_001304717.5:c.1256_1257delinsAT NP_001291646.4:p.Pro419His
NM_001304718.2:c.146_147delinsAT NP_001291647.1:p.Pro49His
NM_000314.8:c.737_738delinsAT MANE Select NP_000305.3:p.Pro246His