Canonical Allele Identifier: CA2588321228

Gene: EIF3G P2RY11 PPAN-P2RY11

Linked Data

• gnomAD v4: 19-10115063-GCTGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115066_10115069del , CM000681.2:g.10115066_10115069del	GRCh38
NC_000019.9:g.10225742_10225745del , CM000681.1:g.10225742_10225745del	GRCh37
NC_000019.8:g.10086742_10086745del	NCBI36
NG_047007.1:g.8546_8549del
NG_051197.1:g.9858_9861del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.*47_*50del (EIF3G) MANE Select	ENSP00000253108.3:n.*47_*50del
ENST00000321826.5:c.*328_*331del (P2RY11) MANE Select	ENSP00000323872.4:n.*328_*331del
ENST00000253108.8:c.*47_*50del (EIF3G)	ENSP00000253108.3:n.*47_*50del
ENST00000321826.4:c.*328_*331del (P2RY11)	ENSP00000323872.4:n.*328_*331del
ENST00000590158.1:n.1029_1032del (EIF3G)
ENST00000593054.5:c.404_407del (EIF3G)	ENSP00000467187.1:n.404_407del
NM_001040664.2:c.*328_*331del (PPAN-P2RY11)	NP_001035754.1:n.*328_*331del
NM_001198690.1:c.*1212_*1215del (PPAN-P2RY11)	NP_001185619.1:n.*1212_*1215del
NM_002566.4:c.*328_*331del (P2RY11)	NP_002557.2:n.*328_*331del
NM_003755.3:c.*47_*50del (EIF3G)	NP_003746.2:n.*47_*50del
NM_003755.4:c.*47_*50del (EIF3G)	NP_003746.2:n.*47_*50del
NM_002566.5:c.*328_*331del (P2RY11) MANE Select	NP_002557.2:n.*328_*331del
NM_003755.5:c.*47_*50del (EIF3G) MANE Select	NP_003746.2:n.*47_*50del
NM_001040664.3:c.*328_*331del (PPAN-P2RY11)	NP_001035754.1:n.*328_*331del
NM_001198690.2:c.*1212_*1215del (PPAN-P2RY11)	NP_001185619.1:n.*1212_*1215del