Canonical Allele Identifier: CA2322270125
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115229T= , CM000681.2:g.10115229T= GRCh38
NC_000019.9:g.10225905T= , CM000681.1:g.10225905T= GRCh37
NC_000019.8:g.10086905T= NCBI36
NG_047007.1:g.8709T=
NG_051197.1:g.9696A=

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.948-100A= (EIF3G) MANE Select ENSP00000253108.3:n.948-100A=
ENST00000321826.5:c.*491T= (P2RY11) MANE Select ENSP00000323872.4:n.*491T=
ENST00000253108.8:c.948-100A= (EIF3G) ENSP00000253108.3:n.948-100A=
ENST00000321826.4:c.*491T= (P2RY11) ENSP00000323872.4:n.*491T=
ENST00000590158.1:n.967-100A= (EIF3G)
ENST00000593054.5:c.342-100A= (EIF3G) ENSP00000467187.1:n.342-100A=
NM_001040664.2:c.*491T= (PPAN-P2RY11) NP_001035754.1:n.*491T=
NM_001198690.1:c.*1375T= (PPAN-P2RY11) NP_001185619.1:n.*1375T=
NM_002566.4:c.*491T= (P2RY11) NP_002557.2:n.*491T=
NM_003755.3:c.948-100A= (EIF3G) NP_003746.2:n.948-100A=
NM_003755.4:c.948-100A= (EIF3G) NP_003746.2:n.948-100A=
NM_002566.5:c.*491T= (P2RY11) MANE Select NP_002557.2:n.*491T=
NM_003755.5:c.948-100A= (EIF3G) MANE Select NP_003746.2:n.948-100A=
NM_001040664.3:c.*491T= (PPAN-P2RY11) NP_001035754.1:n.*491T=
NM_001198690.2:c.*1375T= (PPAN-P2RY11) NP_001185619.1:n.*1375T=