Canonical Allele Identifier: CA2588321188
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115016_10115018del , CM000681.2:g.10115016_10115018del GRCh38
NC_000019.9:g.10225692_10225694del , CM000681.1:g.10225692_10225694del GRCh37
NC_000019.8:g.10086692_10086694del NCBI36
NG_047007.1:g.8496_8498del
NG_051197.1:g.9907_9909del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.*96_*98del (EIF3G) MANE Select ENSP00000253108.3:n.*96_*98del
ENST00000321826.5:c.*278_*280del (P2RY11) MANE Select ENSP00000323872.4:n.*278_*280del
ENST00000321826.4:c.*278_*280del (P2RY11) ENSP00000323872.4:n.*278_*280del
NM_001040664.2:c.*278_*280del (PPAN-P2RY11) NP_001035754.1:n.*278_*280del
NM_001198690.1:c.*1162_*1164del (PPAN-P2RY11) NP_001185619.1:n.*1162_*1164del
NM_002566.4:c.*278_*280del (P2RY11) NP_002557.2:n.*278_*280del
NM_003755.3:c.*96_*98del (EIF3G) NP_003746.2:n.*96_*98del
NM_003755.4:c.*96_*98del (EIF3G) NP_003746.2:n.*96_*98del
NM_002566.5:c.*278_*280del (P2RY11) MANE Select NP_002557.2:n.*278_*280del
NM_003755.5:c.*96_*98del (EIF3G) MANE Select NP_003746.2:n.*96_*98del
NM_001040664.3:c.*278_*280del (PPAN-P2RY11) NP_001035754.1:n.*278_*280del
NM_001198690.2:c.*1162_*1164del (PPAN-P2RY11) NP_001185619.1:n.*1162_*1164del