Canonical Allele Identifier: CA2322270174
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115310A= , CM000681.2:g.10115310A= GRCh38
NC_000019.9:g.10225986A= , CM000681.1:g.10225986A= GRCh37
NC_000019.8:g.10086986A= NCBI36
NG_047007.1:g.8790A=
NG_051197.1:g.9615T=

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+169T= (EIF3G) MANE Select ENSP00000253108.3:n.947+169T=
ENST00000321826.5:c.*572A= (P2RY11) MANE Select ENSP00000323872.4:n.*572A=
ENST00000253108.8:c.947+169T= (EIF3G) ENSP00000253108.3:n.947+169T=
ENST00000321826.4:c.*572A= (P2RY11) ENSP00000323872.4:n.*572A=
ENST00000590158.1:n.966+169T= (EIF3G)
ENST00000593054.5:c.341+169T= (EIF3G) ENSP00000467187.1:n.341+169T=
NM_001040664.2:c.*572A= (PPAN-P2RY11) NP_001035754.1:n.*572A=
NM_001198690.1:c.*1456A= (PPAN-P2RY11) NP_001185619.1:n.*1456A=
NM_002566.4:c.*572A= (P2RY11) NP_002557.2:n.*572A=
NM_003755.3:c.947+169T= (EIF3G) NP_003746.2:n.947+169T=
NM_003755.4:c.947+169T= (EIF3G) NP_003746.2:n.947+169T=
NM_002566.5:c.*572A= (P2RY11) MANE Select NP_002557.2:n.*572A=
NM_003755.5:c.947+169T= (EIF3G) MANE Select NP_003746.2:n.947+169T=
NM_001040664.3:c.*572A= (PPAN-P2RY11) NP_001035754.1:n.*572A=
NM_001198690.2:c.*1456A= (PPAN-P2RY11) NP_001185619.1:n.*1456A=