Canonical Allele Identifier: CA2588321297
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115225_10115226insAAGC , CM000681.2:g.10115225_10115226insAAGC GRCh38
NC_000019.9:g.10225901_10225902insAAGC , CM000681.1:g.10225901_10225902insAAGC GRCh37
NC_000019.8:g.10086901_10086902insAAGC NCBI36
NG_047007.1:g.8705_8706insAAGC
NG_051197.1:g.9699_9700insGCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.948-97_948-96insGCTT (EIF3G) MANE Select ENSP00000253108.3:n.948-97_948-96insGCTT
ENST00000321826.5:c.*487_*488insAAGC (P2RY11) MANE Select ENSP00000323872.4:n.*487_*488insAAGC
ENST00000253108.8:c.948-97_948-96insGCTT (EIF3G) ENSP00000253108.3:n.948-97_948-96insGCTT
ENST00000321826.4:c.*487_*488insAAGC (P2RY11) ENSP00000323872.4:n.*487_*488insAAGC
ENST00000590158.1:n.967-97_967-96insGCTT (EIF3G)
ENST00000593054.5:c.342-97_342-96insGCTT (EIF3G) ENSP00000467187.1:n.342-97_342-96insGCTT
NM_001040664.2:c.*487_*488insAAGC (PPAN-P2RY11) NP_001035754.1:n.*487_*488insAAGC
NM_001198690.1:c.*1371_*1372insAAGC (PPAN-P2RY11) NP_001185619.1:n.*1371_*1372insAAGC
NM_002566.4:c.*487_*488insAAGC (P2RY11) NP_002557.2:n.*487_*488insAAGC
NM_003755.3:c.948-97_948-96insGCTT (EIF3G) NP_003746.2:n.948-97_948-96insGCTT
NM_003755.4:c.948-97_948-96insGCTT (EIF3G) NP_003746.2:n.948-97_948-96insGCTT
NM_002566.5:c.*487_*488insAAGC (P2RY11) MANE Select NP_002557.2:n.*487_*488insAAGC
NM_003755.5:c.948-97_948-96insGCTT (EIF3G) MANE Select NP_003746.2:n.948-97_948-96insGCTT
NM_001040664.3:c.*487_*488insAAGC (PPAN-P2RY11) NP_001035754.1:n.*487_*488insAAGC
NM_001198690.2:c.*1371_*1372insAAGC (PPAN-P2RY11) NP_001185619.1:n.*1371_*1372insAAGC