Canonical Allele Identifier: CA891840938
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958002_87958003delinsCG , CM000672.2:g.87958002_87958003delinsCG GRCh38
NC_000010.10:g.89717759_89717760delinsCG , CM000672.1:g.89717759_89717760delinsCG GRCh37
NC_000010.9:g.89707739_89707740delinsCG NCBI36
NG_007466.2:g.99564_99565delinsCG , LRG_311:g.99564_99565delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.784_785delinsCG ENSP00000514759.2:p.Asn262Arg
ENST00000710265.1:c.784_785delinsCG ENSP00000518161.1:p.Asn262Arg
ENST00000472832.3:c.784_785delinsCG ENSP00000483066.2:p.Asn262Arg
ENST00000688158.2:n.1519_1520delinsCG
ENST00000688922.2:c.*614_*615delinsCG ENSP00000508742.2:n.*614_*615delinsCG
ENST00000700021.1:c.739_740delinsCG ENSP00000514757.1:p.Asn247Arg
ENST00000700022.1:c.*123_*124delinsCG ENSP00000514758.1:n.*123_*124delinsCG
ENST00000700023.1:n.1942_1943delinsCG
ENST00000700024.1:n.2176_2177delinsCG
ENST00000700025.1:n.1553_1554delinsCG
ENST00000700026.1:n.421_422delinsCG
ENST00000700029.1:c.618_619delinsCG
ENST00000706954.1:c.784_785delinsCG ENSP00000516674.1:p.Asn262Arg
ENST00000706955.1:c.*819_*820delinsCG ENSP00000516675.1:n.*819_*820delinsCG
ENST00000686459.1:c.*370_*371delinsCG ENSP00000508909.1:n.*370_*371delinsCG
ENST00000688158.1:c.*895_*896delinsCG ENSP00000509254.1:n.*895_*896delinsCG
ENST00000688308.1:c.784_785delinsCG ENSP00000508752.1:p.Asn262Arg
ENST00000688922.1:c.705_706delinsCG
ENST00000693560.1:c.1303_1304delinsCG ENSP00000509861.1:p.Asn435Arg
ENST00000371953.8:c.784_785delinsCG MANE Select ENSP00000361021.3:p.Asn262Arg
ENST00000371953.7:c.784_785delinsCG ENSP00000361021.3:p.Asn262Arg
ENST00000472832.2:c.211_212delinsCG ENSP00000483066.1:p.Asn71Arg
NM_000314.5:c.784_785delinsCG NP_000305.3:p.Asn262Arg
NM_000314.6:c.784_785delinsCG NP_000305.3:p.Asn262Arg
NM_001304717.2:c.1303_1304delinsCG NP_001291646.2:p.Asn435Arg
NM_001304718.1:c.193_194delinsCG NP_001291647.1:p.Asn65Arg
XM_006717926.2:c.739_740delinsCG XP_006717989.1:p.Asn247Arg
XM_011539981.1:c.784_785delinsCG XP_011538283.1:p.Asn262Arg
XM_011539982.1:c.688_689delinsCG XP_011538284.1:p.Asn230Arg
XR_945791.1:n.1354_1355delinsCG
NM_000314.7:c.784_785delinsCG NP_000305.3:p.Asn262Arg
NM_001304717.5:c.1303_1304delinsCG NP_001291646.4:p.Asn435Arg
NM_001304718.2:c.193_194delinsCG NP_001291647.1:p.Asn65Arg
NM_000314.8:c.784_785delinsCG MANE Select NP_000305.3:p.Asn262Arg