Canonical Allele Identifier: CA631444949
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs1250256659

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115285C>T , CM000681.2:g.10115285C>T GRCh38
NC_000019.9:g.10225961C>T , CM000681.1:g.10225961C>T GRCh37
NC_000019.8:g.10086961C>T NCBI36
NG_047007.1:g.8765C>T
NG_051197.1:g.9640G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.948-156G>A (EIF3G) MANE Select ENSP00000253108.3:n.948-156G>A
ENST00000321826.5:c.*547C>T (P2RY11) MANE Select ENSP00000323872.4:n.*547C>T
ENST00000253108.8:c.948-156G>A (EIF3G) ENSP00000253108.3:n.948-156G>A
ENST00000321826.4:c.*547C>T (P2RY11) ENSP00000323872.4:n.*547C>T
ENST00000590158.1:n.967-156G>A (EIF3G)
ENST00000593054.5:c.342-156G>A (EIF3G) ENSP00000467187.1:n.342-156G>A
NM_001040664.2:c.*547C>T (PPAN-P2RY11) NP_001035754.1:n.*547C>T
NM_001198690.1:c.*1431C>T (PPAN-P2RY11) NP_001185619.1:n.*1431C>T
NM_002566.4:c.*547C>T (P2RY11) NP_002557.2:n.*547C>T
NM_003755.3:c.948-156G>A (EIF3G) NP_003746.2:n.948-156G>A
NM_003755.4:c.948-156G>A (EIF3G) NP_003746.2:n.948-156G>A
NM_002566.5:c.*547C>T (P2RY11) MANE Select NP_002557.2:n.*547C>T
NM_003755.5:c.948-156G>A (EIF3G) MANE Select NP_003746.2:n.948-156G>A
NM_001040664.3:c.*547C>T (PPAN-P2RY11) NP_001035754.1:n.*547C>T
NM_001198690.2:c.*1431C>T (PPAN-P2RY11) NP_001185619.1:n.*1431C>T