Canonical Allele Identifier: CA2322269976

Gene: EIF3G P2RY11 PPAN-P2RY11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115033T= , CM000681.2:g.10115033T=	GRCh38
NC_000019.9:g.10225709T= , CM000681.1:g.10225709T=	GRCh37
NC_000019.8:g.10086709T=	NCBI36
NG_047007.1:g.8513T=
NG_051197.1:g.9892A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.*81A= (EIF3G) MANE Select	ENSP00000253108.3:n.*81A=
ENST00000321826.5:c.*295T= (P2RY11) MANE Select	ENSP00000323872.4:n.*295T=
ENST00000253108.8:c.*81A= (EIF3G)	ENSP00000253108.3:n.*81A=
ENST00000321826.4:c.*295T= (P2RY11)	ENSP00000323872.4:n.*295T=
ENST00000593054.5:c.438A= (EIF3G)	ENSP00000467187.1:n.438A=
NM_001040664.2:c.*295T= (PPAN-P2RY11)	NP_001035754.1:n.*295T=
NM_001198690.1:c.*1179T= (PPAN-P2RY11)	NP_001185619.1:n.*1179T=
NM_002566.4:c.*295T= (P2RY11)	NP_002557.2:n.*295T=
NM_003755.3:c.*81A= (EIF3G)	NP_003746.2:n.*81A=
NM_003755.4:c.*81A= (EIF3G)	NP_003746.2:n.*81A=
NM_002566.5:c.*295T= (P2RY11) MANE Select	NP_002557.2:n.*295T=
NM_003755.5:c.*81A= (EIF3G) MANE Select	NP_003746.2:n.*81A=
NM_001040664.3:c.*295T= (PPAN-P2RY11)	NP_001035754.1:n.*295T=
NM_001198690.2:c.*1179T= (PPAN-P2RY11)	NP_001185619.1:n.*1179T=