Canonical Allele Identifier: CA2588321429
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115345_10115348dup , CM000681.2:g.10115345_10115348dup GRCh38
NC_000019.9:g.10226021_10226024dup , CM000681.1:g.10226021_10226024dup GRCh37
NC_000019.8:g.10087021_10087024dup NCBI36
NG_047007.1:g.8825_8828dup
NG_051197.1:g.9579_9582dup

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+133_947+136dup (EIF3G) MANE Select ENSP00000253108.3:n.947+133_947+136dup
ENST00000321826.5:c.*607_*610dup (P2RY11) MANE Select ENSP00000323872.4:n.*607_*610dup
ENST00000253108.8:c.947+133_947+136dup (EIF3G) ENSP00000253108.3:n.947+133_947+136dup
ENST00000321826.4:c.*607_*610dup (P2RY11) ENSP00000323872.4:n.*607_*610dup
ENST00000590158.1:n.966+133_966+136dup (EIF3G)
ENST00000593054.5:c.341+133_341+136dup (EIF3G) ENSP00000467187.1:n.341+133_341+136dup
NM_001040664.2:c.*607_*610dup (PPAN-P2RY11) NP_001035754.1:n.*607_*610dup
NM_001198690.1:c.*1491_*1494dup (PPAN-P2RY11) NP_001185619.1:n.*1491_*1494dup
NM_002566.4:c.*607_*610dup (P2RY11) NP_002557.2:n.*607_*610dup
NM_003755.3:c.947+133_947+136dup (EIF3G) NP_003746.2:n.947+133_947+136dup
NM_003755.4:c.947+133_947+136dup (EIF3G) NP_003746.2:n.947+133_947+136dup
NM_002566.5:c.*607_*610dup (P2RY11) MANE Select NP_002557.2:n.*607_*610dup
NM_003755.5:c.947+133_947+136dup (EIF3G) MANE Select NP_003746.2:n.947+133_947+136dup
NM_001040664.3:c.*607_*610dup (PPAN-P2RY11) NP_001035754.1:n.*607_*610dup
NM_001198690.2:c.*1491_*1494dup (PPAN-P2RY11) NP_001185619.1:n.*1491_*1494dup