Canonical Allele Identifier: CA891837009
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965300_87965301delinsGG , CM000672.2:g.87965300_87965301delinsGG GRCh38
NC_000010.10:g.89725057_89725058delinsGG , CM000672.1:g.89725057_89725058delinsGG GRCh37
NC_000010.9:g.89715037_89715038delinsGG NCBI36
NG_007466.2:g.106862_106863delinsGG , LRG_311:g.106862_106863delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1133_1134delinsGG ENSP00000514759.2:p.Phe378Trp
ENST00000710265.1:c.*69_*70delinsGG ENSP00000518161.1:n.*69_*70delinsGG
ENST00000688158.2:n.1775_1776delinsGG
ENST00000688922.2:c.*870_*871delinsGG ENSP00000508742.2:n.*870_*871delinsGG
ENST00000700021.1:c.995_996delinsGG ENSP00000514757.1:p.Phe332Trp
ENST00000700022.1:c.*379_*380delinsGG ENSP00000514758.1:n.*379_*380delinsGG
ENST00000700023.1:n.2198_2199delinsGG
ENST00000700024.1:n.2432_2433delinsGG
ENST00000706954.1:c.1040_1041delinsGG ENSP00000516674.1:p.Phe347Trp
ENST00000706955.1:c.*1075_*1076delinsGG ENSP00000516675.1:n.*1075_*1076delinsGG
ENST00000686459.1:c.*626_*627delinsGG ENSP00000508909.1:n.*626_*627delinsGG
ENST00000688158.1:c.*1151_*1152delinsGG ENSP00000509254.1:n.*1151_*1152delinsGG
ENST00000688308.1:c.1040_1041delinsGG ENSP00000508752.1:p.Phe347Trp
ENST00000688922.1:c.961_962delinsGG
ENST00000693560.1:c.1559_1560delinsGG ENSP00000509861.1:p.Phe520Trp
ENST00000371953.8:c.1040_1041delinsGG MANE Select ENSP00000361021.3:p.Phe347Trp
ENST00000371953.7:c.1040_1041delinsGG ENSP00000361021.3:p.Phe347Trp
NM_000314.5:c.1040_1041delinsGG NP_000305.3:p.Phe347Trp
NM_000314.6:c.1040_1041delinsGG NP_000305.3:p.Phe347Trp
NM_001304717.2:c.1559_1560delinsGG NP_001291646.2:p.Phe520Trp
NM_001304718.1:c.449_450delinsGG NP_001291647.1:p.Phe150Trp
XM_006717926.2:c.995_996delinsGG XP_006717989.1:p.Phe332Trp
XM_011539982.1:c.944_945delinsGG XP_011538284.1:p.Phe315Trp
XR_945791.1:n.1610_1611delinsGG
NM_000314.7:c.1040_1041delinsGG NP_000305.3:p.Phe347Trp
NM_001304717.5:c.1559_1560delinsGG NP_001291646.4:p.Phe520Trp
NM_001304718.2:c.449_450delinsGG NP_001291647.1:p.Phe150Trp
NM_000314.8:c.1040_1041delinsGG MANE Select NP_000305.3:p.Phe347Trp