Canonical Allele Identifier: CA2588321471

Gene: EIF3G P2RY11 PPAN-P2RY11

Linked Data

• gnomAD v4: 19-10115368-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115368A>G , CM000681.2:g.10115368A>G	GRCh38
NC_000019.9:g.10226044A>G , CM000681.1:g.10226044A>G	GRCh37
NC_000019.8:g.10087044A>G	NCBI36
NG_047007.1:g.8848A>G
NG_051197.1:g.9557T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.947+111T>C (EIF3G) MANE Select	ENSP00000253108.3:n.947+111T>C
ENST00000321826.5:c.*630A>G (P2RY11) MANE Select	ENSP00000323872.4:n.*630A>G
ENST00000253108.8:c.947+111T>C (EIF3G)	ENSP00000253108.3:n.947+111T>C
ENST00000321826.4:c.*630A>G (P2RY11)	ENSP00000323872.4:n.*630A>G
ENST00000590158.1:n.966+111T>C (EIF3G)
ENST00000593054.5:c.341+111T>C (EIF3G)	ENSP00000467187.1:n.341+111T>C
NM_001040664.2:c.*630A>G (PPAN-P2RY11)	NP_001035754.1:n.*630A>G
NM_001198690.1:c.*1514A>G (PPAN-P2RY11)	NP_001185619.1:n.*1514A>G
NM_002566.4:c.*630A>G (P2RY11)	NP_002557.2:n.*630A>G
NM_003755.3:c.947+111T>C (EIF3G)	NP_003746.2:n.947+111T>C
NM_003755.4:c.947+111T>C (EIF3G)	NP_003746.2:n.947+111T>C
NM_002566.5:c.*630A>G (P2RY11) MANE Select	NP_002557.2:n.*630A>G
NM_003755.5:c.947+111T>C (EIF3G) MANE Select	NP_003746.2:n.947+111T>C
NM_001040664.3:c.*630A>G (PPAN-P2RY11)	NP_001035754.1:n.*630A>G
NM_001198690.2:c.*1514A>G (PPAN-P2RY11)	NP_001185619.1:n.*1514A>G