Canonical Allele Identifier: CA2322269964

Gene: EIF3G P2RY11 PPAN-P2RY11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115019A= , CM000681.2:g.10115019A=	GRCh38
NC_000019.9:g.10225695A= , CM000681.1:g.10225695A=	GRCh37
NC_000019.8:g.10086695A=	NCBI36
NG_047007.1:g.8499A=
NG_051197.1:g.9906T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.*95T= (EIF3G) MANE Select	ENSP00000253108.3:n.*95T=
ENST00000321826.5:c.*281A= (P2RY11) MANE Select	ENSP00000323872.4:n.*281A=
ENST00000253108.8:c.*95T= (EIF3G)	ENSP00000253108.3:n.*95T=
ENST00000321826.4:c.*281A= (P2RY11)	ENSP00000323872.4:n.*281A=
ENST00000593054.5:c.452T= (EIF3G)	ENSP00000467187.1:n.452T=
NM_001040664.2:c.*281A= (PPAN-P2RY11)	NP_001035754.1:n.*281A=
NM_001198690.1:c.*1165A= (PPAN-P2RY11)	NP_001185619.1:n.*1165A=
NM_002566.4:c.*281A= (P2RY11)	NP_002557.2:n.*281A=
NM_003755.3:c.*95T= (EIF3G)	NP_003746.2:n.*95T=
NM_003755.4:c.*95T= (EIF3G)	NP_003746.2:n.*95T=
NM_002566.5:c.*281A= (P2RY11) MANE Select	NP_002557.2:n.*281A=
NM_003755.5:c.*95T= (EIF3G) MANE Select	NP_003746.2:n.*95T=
NM_001040664.3:c.*281A= (PPAN-P2RY11)	NP_001035754.1:n.*281A=
NM_001198690.2:c.*1165A= (PPAN-P2RY11)	NP_001185619.1:n.*1165A=