Canonical Allele Identifier: CA2588321204

Gene: EIF3G P2RY11 PPAN-P2RY11

Linked Data

• gnomAD v4: 19-10115028-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115029dup , CM000681.2:g.10115029dup	GRCh38
NC_000019.9:g.10225705dup , CM000681.1:g.10225705dup	GRCh37
NC_000019.8:g.10086705dup	NCBI36
NG_047007.1:g.8509dup
NG_051197.1:g.9896dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.*85dup (EIF3G) MANE Select	ENSP00000253108.3:n.*85dup
ENST00000321826.5:c.*291dup (P2RY11) MANE Select	ENSP00000323872.4:n.*291dup
ENST00000253108.8:c.*85dup (EIF3G)	ENSP00000253108.3:n.*85dup
ENST00000321826.4:c.*291dup (P2RY11)	ENSP00000323872.4:n.*291dup
ENST00000593054.5:c.442dup (EIF3G)	ENSP00000467187.1:n.442dup
NM_001040664.2:c.*291dup (PPAN-P2RY11)	NP_001035754.1:n.*291dup
NM_001198690.1:c.*1175dup (PPAN-P2RY11)	NP_001185619.1:n.*1175dup
NM_002566.4:c.*291dup (P2RY11)	NP_002557.2:n.*291dup
NM_003755.3:c.*85dup (EIF3G)	NP_003746.2:n.*85dup
NM_003755.4:c.*85dup (EIF3G)	NP_003746.2:n.*85dup
NM_002566.5:c.*291dup (P2RY11) MANE Select	NP_002557.2:n.*291dup
NM_003755.5:c.*85dup (EIF3G) MANE Select	NP_003746.2:n.*85dup
NM_001040664.3:c.*291dup (PPAN-P2RY11)	NP_001035754.1:n.*291dup
NM_001198690.2:c.*1175dup (PPAN-P2RY11)	NP_001185619.1:n.*1175dup