Canonical Allele Identifier: CA2322270209

Gene: EIF3G P2RY11 PPAN-P2RY11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115360C= , CM000681.2:g.10115360C=	GRCh38
NC_000019.9:g.10226036C= , CM000681.1:g.10226036C=	GRCh37
NC_000019.8:g.10087036C=	NCBI36
NG_047007.1:g.8840C=
NG_051197.1:g.9565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.947+119G= (EIF3G) MANE Select	ENSP00000253108.3:n.947+119G=
ENST00000321826.5:c.*622C= (P2RY11) MANE Select	ENSP00000323872.4:n.*622C=
ENST00000253108.8:c.947+119G= (EIF3G)	ENSP00000253108.3:n.947+119G=
ENST00000321826.4:c.*622C= (P2RY11)	ENSP00000323872.4:n.*622C=
ENST00000590158.1:n.966+119G= (EIF3G)
ENST00000593054.5:c.341+119G= (EIF3G)	ENSP00000467187.1:n.341+119G=
NM_001040664.2:c.*622C= (PPAN-P2RY11)	NP_001035754.1:n.*622C=
NM_001198690.1:c.*1506C= (PPAN-P2RY11)	NP_001185619.1:n.*1506C=
NM_002566.4:c.*622C= (P2RY11)	NP_002557.2:n.*622C=
NM_003755.3:c.947+119G= (EIF3G)	NP_003746.2:n.947+119G=
NM_003755.4:c.947+119G= (EIF3G)	NP_003746.2:n.947+119G=
NM_002566.5:c.*622C= (P2RY11) MANE Select	NP_002557.2:n.*622C=
NM_003755.5:c.947+119G= (EIF3G) MANE Select	NP_003746.2:n.947+119G=
NM_001040664.3:c.*622C= (PPAN-P2RY11)	NP_001035754.1:n.*622C=
NM_001198690.2:c.*1506C= (PPAN-P2RY11)	NP_001185619.1:n.*1506C=