Canonical Allele Identifier: CA891840931
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957999_87958000delinsGG , CM000672.2:g.87957999_87958000delinsGG GRCh38
NC_000010.10:g.89717756_89717757delinsGG , CM000672.1:g.89717756_89717757delinsGG GRCh37
NC_000010.9:g.89707736_89707737delinsGG NCBI36
NG_007466.2:g.99561_99562delinsGG , LRG_311:g.99561_99562delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.781_782delinsGG ENSP00000514759.2:p.Gln261Gly
ENST00000710265.1:c.781_782delinsGG ENSP00000518161.1:p.Gln261Gly
ENST00000472832.3:c.781_782delinsGG ENSP00000483066.2:p.Gln261Gly
ENST00000688158.2:n.1516_1517delinsGG
ENST00000688922.2:c.*611_*612delinsGG ENSP00000508742.2:n.*611_*612delinsGG
ENST00000700021.1:c.736_737delinsGG ENSP00000514757.1:p.Gln246Gly
ENST00000700022.1:c.*120_*121delinsGG ENSP00000514758.1:n.*120_*121delinsGG
ENST00000700023.1:n.1939_1940delinsGG
ENST00000700024.1:n.2173_2174delinsGG
ENST00000700025.1:n.1550_1551delinsGG
ENST00000700026.1:n.418_419delinsGG
ENST00000700029.1:c.615_616delinsGG
ENST00000706954.1:c.781_782delinsGG ENSP00000516674.1:p.Gln261Gly
ENST00000706955.1:c.*816_*817delinsGG ENSP00000516675.1:n.*816_*817delinsGG
ENST00000686459.1:c.*367_*368delinsGG ENSP00000508909.1:n.*367_*368delinsGG
ENST00000688158.1:c.*892_*893delinsGG ENSP00000509254.1:n.*892_*893delinsGG
ENST00000688308.1:c.781_782delinsGG ENSP00000508752.1:p.Gln261Gly
ENST00000688922.1:c.702_703delinsGG
ENST00000693560.1:c.1300_1301delinsGG ENSP00000509861.1:p.Gln434Gly
ENST00000371953.8:c.781_782delinsGG MANE Select ENSP00000361021.3:p.Gln261Gly
ENST00000371953.7:c.781_782delinsGG ENSP00000361021.3:p.Gln261Gly
ENST00000472832.2:c.208_209delinsGG ENSP00000483066.1:p.Gln70Gly
NM_000314.5:c.781_782delinsGG NP_000305.3:p.Gln261Gly
NM_000314.6:c.781_782delinsGG NP_000305.3:p.Gln261Gly
NM_001304717.2:c.1300_1301delinsGG NP_001291646.2:p.Gln434Gly
NM_001304718.1:c.190_191delinsGG NP_001291647.1:p.Gln64Gly
XM_006717926.2:c.736_737delinsGG XP_006717989.1:p.Gln246Gly
XM_011539981.1:c.781_782delinsGG XP_011538283.1:p.Gln261Gly
XM_011539982.1:c.685_686delinsGG XP_011538284.1:p.Gln229Gly
XR_945791.1:n.1351_1352delinsGG
NM_000314.7:c.781_782delinsGG NP_000305.3:p.Gln261Gly
NM_001304717.5:c.1300_1301delinsGG NP_001291646.4:p.Gln434Gly
NM_001304718.2:c.190_191delinsGG NP_001291647.1:p.Gln64Gly
NM_000314.8:c.781_782delinsGG MANE Select NP_000305.3:p.Gln261Gly