Canonical Allele Identifier: CA2735551086
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs2145224788
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115133_10115134insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC , CM000681.2:g.10115133_10115134insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC GRCh38
NC_000019.9:g.10225809_10225810insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC , CM000681.1:g.10225809_10225810insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC GRCh37
NC_000019.8:g.10086809_10086810insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC NCBI36
NG_047007.1:g.8613_8614insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC
NG_051197.1:g.9791_9792insGGCTTTGGCTACGACCACCTCATCCTCAACGTCGAGTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTCGAGTGGG (EIF3G) MANE Select ENSP00000253108.3:n.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTC...
ENST00000321826.5:c.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC (P2RY11) MANE Select ENSP00000323872.4:n.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCG...
ENST00000253108.8:c.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTCGAGTGGG (EIF3G) ENSP00000253108.3:n.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTC...
ENST00000321826.4:c.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC (P2RY11) ENSP00000323872.4:n.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCG...
ENST00000590158.1:n.967-5_967-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTCGAGTGGG (EIF3G)
ENST00000593054.5:c.342-5_342-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTCGAGTGGG (EIF3G) ENSP00000467187.1:n.342-5_342-4insGGCTTTGGCTACGACCACCTCATCCTC...
NM_001040664.2:c.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC (PPAN-P2RY11) NP_001035754.1:n.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAG...
NM_001198690.1:c.*1279_*1280insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC (PPAN-P2RY11) NP_001185619.1:n.*1279_*1280insCCCACTCGACGTTGAGGATGAGGTGGTCGT...
NM_002566.4:c.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC (P2RY11) NP_002557.2:n.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCA...
NM_003755.3:c.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTCGAGTGGG (EIF3G) NP_003746.2:n.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTC...
NM_003755.4:c.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTCGAGTGGG (EIF3G) NP_003746.2:n.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTC...
NM_002566.5:c.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC (P2RY11) MANE Select NP_002557.2:n.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCA...
NM_003755.5:c.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTCGAGTGGG (EIF3G) MANE Select NP_003746.2:n.948-5_948-4insGGCTTTGGCTACGACCACCTCATCCTCAACGTC...
NM_001040664.3:c.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC (PPAN-P2RY11) NP_001035754.1:n.*395_*396insCCCACTCGACGTTGAGGATGAGGTGGTCGTAG...
NM_001198690.2:c.*1279_*1280insCCCACTCGACGTTGAGGATGAGGTGGTCGTAGCCAAAGCC (PPAN-P2RY11) NP_001185619.1:n.*1279_*1280insCCCACTCGACGTTGAGGATGAGGTGGTCGT...
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