Canonical Allele Identifier: CA891837575
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933138_87933139delinsCC , CM000672.2:g.87933138_87933139delinsCC GRCh38
NC_000010.10:g.89692895_89692896delinsCC , CM000672.1:g.89692895_89692896delinsCC GRCh37
NC_000010.9:g.89682875_89682876delinsCC NCBI36
NG_007466.2:g.74700_74701delinsCC , LRG_311:g.74700_74701delinsCC

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.379_380delinsCC ENSP00000514759.2:p.Gly127Pro
ENST00000710265.1:c.379_380delinsCC ENSP00000518161.1:p.Gly127Pro
ENST00000472832.3:c.379_380delinsCC ENSP00000483066.2:p.Gly127Pro
ENST00000688158.2:n.1114_1115delinsCC
ENST00000688922.2:c.*209_*210delinsCC ENSP00000508742.2:n.*209_*210delinsCC
ENST00000700021.1:c.334_335delinsCC ENSP00000514757.1:p.Gly112Pro
ENST00000700022.1:c.379_380delinsCC ENSP00000514758.1:p.Gly127Pro
ENST00000700029.1:c.213_214delinsCC
ENST00000706954.1:c.379_380delinsCC ENSP00000516674.1:p.Gly127Pro
ENST00000706955.1:c.*414_*415delinsCC ENSP00000516675.1:n.*414_*415delinsCC
ENST00000686459.1:c.379_380delinsCC ENSP00000508909.1:p.Gly127Pro
ENST00000688158.1:c.*490_*491delinsCC ENSP00000509254.1:n.*490_*491delinsCC
ENST00000688308.1:c.379_380delinsCC ENSP00000508752.1:p.Gly127Pro
ENST00000688922.1:c.300_301delinsCC
ENST00000693560.1:c.898_899delinsCC ENSP00000509861.1:p.Gly300Pro
ENST00000371953.8:c.379_380delinsCC MANE Select ENSP00000361021.3:p.Gly127Pro
ENST00000371953.7:c.379_380delinsCC ENSP00000361021.3:p.Gly127Pro
ENST00000498703.1:n.205_206delinsCC
ENST00000610634.1:c.277_278delinsCC ENSP00000477517.1:p.Gly93Pro
NM_000314.5:c.379_380delinsCC NP_000305.3:p.Gly127Pro
NM_000314.6:c.379_380delinsCC NP_000305.3:p.Gly127Pro
NM_001304717.2:c.898_899delinsCC NP_001291646.2:p.Gly300Pro
NM_001304718.1:c.-372_-371delinsCC NP_001291647.1:n.-372_-371delinsCC
XM_006717926.2:c.334_335delinsCC XP_006717989.1:p.Gly112Pro
XM_011539981.1:c.379_380delinsCC XP_011538283.1:p.Gly127Pro
XM_011539982.1:c.283_284delinsCC XP_011538284.1:p.Gly95Pro
XR_945789.1:n.1091_1092delinsCC
XR_945790.1:n.1091_1092delinsCC
XR_945791.1:n.1091_1092delinsCC
NM_000314.7:c.379_380delinsCC NP_000305.3:p.Gly127Pro
NM_001304717.5:c.898_899delinsCC NP_001291646.4:p.Gly300Pro
NM_001304718.2:c.-372_-371delinsCC NP_001291647.1:n.-372_-371delinsCC
NM_000314.8:c.379_380delinsCC MANE Select NP_000305.3:p.Gly127Pro