Canonical Allele Identifier: CA891837837
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965396_87965397delinsGG , CM000672.2:g.87965396_87965397delinsGG GRCh38
NC_000010.10:g.89725153_89725154delinsGG , CM000672.1:g.89725153_89725154delinsGG GRCh37
NC_000010.9:g.89715133_89715134delinsGG NCBI36
NG_007466.2:g.106958_106959delinsGG , LRG_311:g.106958_106959delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1229_1230delinsGG ENSP00000514759.2:p.Tyr410Trp
ENST00000710265.1:c.*165_*166delinsGG ENSP00000518161.1:n.*165_*166delinsGG
ENST00000688158.2:n.1871_1872delinsGG
ENST00000688922.2:c.*966_*967delinsGG ENSP00000508742.2:n.*966_*967delinsGG
ENST00000700021.1:c.1091_1092delinsGG ENSP00000514757.1:p.Tyr364Trp
ENST00000700022.1:c.*475_*476delinsGG ENSP00000514758.1:n.*475_*476delinsGG
ENST00000700023.1:n.2294_2295delinsGG
ENST00000700024.1:n.2528_2529delinsGG
ENST00000706954.1:c.1136_1137delinsGG ENSP00000516674.1:p.Tyr379Trp
ENST00000706955.1:c.*1171_*1172delinsGG ENSP00000516675.1:n.*1171_*1172delinsGG
ENST00000686459.1:c.*722_*723delinsGG ENSP00000508909.1:n.*722_*723delinsGG
ENST00000688158.1:c.*1247_*1248delinsGG ENSP00000509254.1:n.*1247_*1248delinsGG
ENST00000688308.1:c.1136_1137delinsGG ENSP00000508752.1:p.Tyr379Trp
ENST00000688922.1:c.1057_1058delinsGG
ENST00000693560.1:c.1655_1656delinsGG ENSP00000509861.1:p.Tyr552Trp
ENST00000371953.8:c.1136_1137delinsGG MANE Select ENSP00000361021.3:p.Tyr379Trp
ENST00000371953.7:c.1136_1137delinsGG ENSP00000361021.3:p.Tyr379Trp
NM_000314.5:c.1136_1137delinsGG NP_000305.3:p.Tyr379Trp
NM_000314.6:c.1136_1137delinsGG NP_000305.3:p.Tyr379Trp
NM_001304717.2:c.1655_1656delinsGG NP_001291646.2:p.Tyr552Trp
NM_001304718.1:c.545_546delinsGG NP_001291647.1:p.Tyr182Trp
XM_006717926.2:c.1091_1092delinsGG XP_006717989.1:p.Tyr364Trp
XM_011539982.1:c.1040_1041delinsGG XP_011538284.1:p.Tyr347Trp
XR_945791.1:n.1706_1707delinsGG
NM_000314.7:c.1136_1137delinsGG NP_000305.3:p.Tyr379Trp
NM_001304717.5:c.1655_1656delinsGG NP_001291646.4:p.Tyr552Trp
NM_001304718.2:c.545_546delinsGG NP_001291647.1:p.Tyr182Trp
NM_000314.8:c.1136_1137delinsGG MANE Select NP_000305.3:p.Tyr379Trp