Canonical Allele Identifier: CA891839863
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957963_87957965delinsCAT , CM000672.2:g.87957963_87957965delinsCAT GRCh38
NC_000010.10:g.89717720_89717722delinsCAT , CM000672.1:g.89717720_89717722delinsCAT GRCh37
NC_000010.9:g.89707700_89707702delinsCAT NCBI36
NG_007466.2:g.99525_99527delinsCAT , LRG_311:g.99525_99527delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.745_747delinsCAT ENSP00000514759.2:p.Val249His
ENST00000710265.1:c.745_747delinsCAT ENSP00000518161.1:p.Val249His
ENST00000472832.3:c.745_747delinsCAT ENSP00000483066.2:p.Val249His
ENST00000688158.2:n.1480_1482delinsCAT
ENST00000688922.2:c.*575_*577delinsCAT ENSP00000508742.2:n.*575_*577delinsCAT
ENST00000700021.1:c.700_702delinsCAT ENSP00000514757.1:p.Val234His
ENST00000700022.1:c.*84_*86delinsCAT ENSP00000514758.1:n.*84_*86delinsCAT
ENST00000700023.1:n.1903_1905delinsCAT
ENST00000700024.1:n.2137_2139delinsCAT
ENST00000700025.1:n.1514_1516delinsCAT
ENST00000700026.1:n.382_384delinsCAT
ENST00000700029.1:c.579_581delinsCAT
ENST00000706954.1:c.745_747delinsCAT ENSP00000516674.1:p.Val249His
ENST00000706955.1:c.*780_*782delinsCAT ENSP00000516675.1:n.*780_*782delinsCAT
ENST00000686459.1:c.*331_*333delinsCAT ENSP00000508909.1:n.*331_*333delinsCAT
ENST00000688158.1:c.*856_*858delinsCAT ENSP00000509254.1:n.*856_*858delinsCAT
ENST00000688308.1:c.745_747delinsCAT ENSP00000508752.1:p.Val249His
ENST00000688922.1:c.666_668delinsCAT
ENST00000693560.1:c.1264_1266delinsCAT ENSP00000509861.1:p.Val422His
ENST00000371953.8:c.745_747delinsCAT MANE Select ENSP00000361021.3:p.Val249His
ENST00000371953.7:c.745_747delinsCAT ENSP00000361021.3:p.Val249His
ENST00000472832.2:c.172_174delinsCAT ENSP00000483066.1:p.Val58His
NM_000314.5:c.745_747delinsCAT NP_000305.3:p.Val249His
NM_000314.6:c.745_747delinsCAT NP_000305.3:p.Val249His
NM_001304717.2:c.1264_1266delinsCAT NP_001291646.2:p.Val422His
NM_001304718.1:c.154_156delinsCAT NP_001291647.1:p.Val52His
XM_006717926.2:c.700_702delinsCAT XP_006717989.1:p.Val234His
XM_011539981.1:c.745_747delinsCAT XP_011538283.1:p.Val249His
XM_011539982.1:c.649_651delinsCAT XP_011538284.1:p.Val217His
XR_945791.1:n.1315_1317delinsCAT
NM_000314.7:c.745_747delinsCAT NP_000305.3:p.Val249His
NM_001304717.5:c.1264_1266delinsCAT NP_001291646.4:p.Val422His
NM_001304718.2:c.154_156delinsCAT NP_001291647.1:p.Val52His
NM_000314.8:c.745_747delinsCAT MANE Select NP_000305.3:p.Val249His