Canonical Allele Identifier: CA2322270033

Gene: EIF3G P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs2089216777
• gnomAD v4: 19-10115100-CAGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115101_10115103del , CM000681.2:g.10115101_10115103del	GRCh38
NC_000019.9:g.10225777_10225779del , CM000681.1:g.10225777_10225779del	GRCh37
NC_000019.8:g.10086777_10086779del	NCBI36
NG_047007.1:g.8581_8583del
NG_051197.1:g.9822_9824del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.*11_*13del (EIF3G) MANE Select	ENSP00000253108.3:n.*11_*13del
ENST00000321826.5:c.*363_*365del (P2RY11) MANE Select	ENSP00000323872.4:n.*363_*365del
ENST00000253108.8:c.*11_*13del (EIF3G)	ENSP00000253108.3:n.*11_*13del
ENST00000321826.4:c.*363_*365del (P2RY11)	ENSP00000323872.4:n.*363_*365del
ENST00000590158.1:n.993_995del (EIF3G)
ENST00000593054.5:c.368_370del (EIF3G)	ENSP00000467187.1:n.368_370del
NM_001040664.2:c.*363_*365del (PPAN-P2RY11)	NP_001035754.1:n.*363_*365del
NM_001198690.1:c.*1247_*1249del (PPAN-P2RY11)	NP_001185619.1:n.*1247_*1249del
NM_002566.4:c.*363_*365del (P2RY11)	NP_002557.2:n.*363_*365del
NM_003755.3:c.*11_*13del (EIF3G)	NP_003746.2:n.*11_*13del
NM_003755.4:c.*11_*13del (EIF3G)	NP_003746.2:n.*11_*13del
NM_002566.5:c.*363_*365del (P2RY11) MANE Select	NP_002557.2:n.*363_*365del
NM_003755.5:c.*11_*13del (EIF3G) MANE Select	NP_003746.2:n.*11_*13del
NM_001040664.3:c.*363_*365del (PPAN-P2RY11)	NP_001035754.1:n.*363_*365del
NM_001198690.2:c.*1247_*1249del (PPAN-P2RY11)	NP_001185619.1:n.*1247_*1249del