Canonical Allele Identifier: CA2813565521

Gene: EIF3G P2RY11 PPAN-P2RY11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115294_10115295insTCT , CM000681.2:g.10115294_10115295insTCT	GRCh38
NC_000019.9:g.10225970_10225971insTCT , CM000681.1:g.10225970_10225971insTCT	GRCh37
NC_000019.8:g.10086970_10086971insTCT	NCBI36
NG_047007.1:g.8774_8775insTCT
NG_051197.1:g.9630_9631insAGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000253108.9:c.948-166_948-165insAGA (EIF3G) MANE Select	ENSP00000253108.3:n.948-166_948-165insAGA
ENST00000321826.5:c.*556_*557insTCT (P2RY11) MANE Select	ENSP00000323872.4:n.*556_*557insTCT
ENST00000253108.8:c.948-166_948-165insAGA (EIF3G)	ENSP00000253108.3:n.948-166_948-165insAGA
ENST00000321826.4:c.*556_*557insTCT (P2RY11)	ENSP00000323872.4:n.*556_*557insTCT
ENST00000590158.1:n.967-166_967-165insAGA (EIF3G)
ENST00000593054.5:c.342-166_342-165insAGA (EIF3G)	ENSP00000467187.1:n.342-166_342-165insAGA
NM_001040664.2:c.*556_*557insTCT (PPAN-P2RY11)	NP_001035754.1:n.*556_*557insTCT
NM_001198690.1:c.*1440_*1441insTCT (PPAN-P2RY11)	NP_001185619.1:n.*1440_*1441insTCT
NM_002566.4:c.*556_*557insTCT (P2RY11)	NP_002557.2:n.*556_*557insTCT
NM_003755.3:c.948-166_948-165insAGA (EIF3G)	NP_003746.2:n.948-166_948-165insAGA
NM_003755.4:c.948-166_948-165insAGA (EIF3G)	NP_003746.2:n.948-166_948-165insAGA
NM_002566.5:c.*556_*557insTCT (P2RY11) MANE Select	NP_002557.2:n.*556_*557insTCT
NM_003755.5:c.948-166_948-165insAGA (EIF3G) MANE Select	NP_003746.2:n.948-166_948-165insAGA
NM_001040664.3:c.*556_*557insTCT (PPAN-P2RY11)	NP_001035754.1:n.*556_*557insTCT
NM_001198690.2:c.*1440_*1441insTCT (PPAN-P2RY11)	NP_001185619.1:n.*1440_*1441insTCT