Canonical Allele Identifier: CA891840136
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958017_87958018delinsTG , CM000672.2:g.87958017_87958018delinsTG GRCh38
NC_000010.10:g.89717774_89717775delinsTG , CM000672.1:g.89717774_89717775delinsTG GRCh37
NC_000010.9:g.89707754_89707755delinsTG NCBI36
NG_007466.2:g.99579_99580delinsTG , LRG_311:g.99579_99580delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.799_800delinsTG ENSP00000514759.2:p.Lys267Trp
ENST00000710265.1:c.799_800delinsTG ENSP00000518161.1:p.Lys267Trp
ENST00000472832.3:c.799_800delinsTG ENSP00000483066.2:p.Lys267Trp
ENST00000688158.2:n.1534_1535delinsTG
ENST00000688922.2:c.*629_*630delinsTG ENSP00000508742.2:n.*629_*630delinsTG
ENST00000700021.1:c.754_755delinsTG ENSP00000514757.1:p.Lys252Trp
ENST00000700022.1:c.*138_*139delinsTG ENSP00000514758.1:n.*138_*139delinsTG
ENST00000700023.1:n.1957_1958delinsTG
ENST00000700024.1:n.2191_2192delinsTG
ENST00000700025.1:n.1568_1569delinsTG
ENST00000700026.1:n.436_437delinsTG
ENST00000700029.1:c.633_634delinsTG
ENST00000706954.1:c.799_800delinsTG ENSP00000516674.1:p.Lys267Trp
ENST00000706955.1:c.*834_*835delinsTG ENSP00000516675.1:n.*834_*835delinsTG
ENST00000686459.1:c.*385_*386delinsTG ENSP00000508909.1:n.*385_*386delinsTG
ENST00000688158.1:c.*910_*911delinsTG ENSP00000509254.1:n.*910_*911delinsTG
ENST00000688308.1:c.799_800delinsTG ENSP00000508752.1:p.Lys267Trp
ENST00000688922.1:c.720_721delinsTG
ENST00000693560.1:c.1318_1319delinsTG ENSP00000509861.1:p.Lys440Trp
ENST00000371953.8:c.799_800delinsTG MANE Select ENSP00000361021.3:p.Lys267Trp
ENST00000371953.7:c.799_800delinsTG ENSP00000361021.3:p.Lys267Trp
ENST00000472832.2:c.226_227delinsTG ENSP00000483066.1:p.Lys76Trp
NM_000314.5:c.799_800delinsTG NP_000305.3:p.Lys267Trp
NM_000314.6:c.799_800delinsTG NP_000305.3:p.Lys267Trp
NM_001304717.2:c.1318_1319delinsTG NP_001291646.2:p.Lys440Trp
NM_001304718.1:c.208_209delinsTG NP_001291647.1:p.Lys70Trp
XM_006717926.2:c.754_755delinsTG XP_006717989.1:p.Lys252Trp
XM_011539981.1:c.799_800delinsTG XP_011538283.1:p.Lys267Trp
XM_011539982.1:c.703_704delinsTG XP_011538284.1:p.Lys235Trp
XR_945791.1:n.1369_1370delinsTG
NM_000314.7:c.799_800delinsTG NP_000305.3:p.Lys267Trp
NM_001304717.5:c.1318_1319delinsTG NP_001291646.4:p.Lys440Trp
NM_001304718.2:c.208_209delinsTG NP_001291647.1:p.Lys70Trp
NM_000314.8:c.799_800delinsTG MANE Select NP_000305.3:p.Lys267Trp