Canonical Allele Identifier: CA2813565527

Gene: EIF3G P2RY11 PPAN-P2RY11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115318_10115319insTCACATT , CM000681.2:g.10115318_10115319insTCACATT	GRCh38
NC_000019.9:g.10225994_10225995insTCACATT , CM000681.1:g.10225994_10225995insTCACATT	GRCh37
NC_000019.8:g.10086994_10086995insTCACATT	NCBI36
NG_047007.1:g.8798_8799insTCACATT
NG_051197.1:g.9606_9607insAATGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.947+160_947+161insAATGTGA (EIF3G) MANE Select	ENSP00000253108.3:n.947+160_947+161insAATGTGA
ENST00000321826.5:c.*580_*581insTCACATT (P2RY11) MANE Select	ENSP00000323872.4:n.*580_*581insTCACATT
ENST00000253108.8:c.947+160_947+161insAATGTGA (EIF3G)	ENSP00000253108.3:n.947+160_947+161insAATGTGA
ENST00000321826.4:c.*580_*581insTCACATT (P2RY11)	ENSP00000323872.4:n.*580_*581insTCACATT
ENST00000590158.1:n.966+160_966+161insAATGTGA (EIF3G)
ENST00000593054.5:c.341+160_341+161insAATGTGA (EIF3G)	ENSP00000467187.1:n.341+160_341+161insAATGTGA
NM_001040664.2:c.*580_*581insTCACATT (PPAN-P2RY11)	NP_001035754.1:n.*580_*581insTCACATT
NM_001198690.1:c.*1464_*1465insTCACATT (PPAN-P2RY11)	NP_001185619.1:n.*1464_*1465insTCACATT
NM_002566.4:c.*580_*581insTCACATT (P2RY11)	NP_002557.2:n.*580_*581insTCACATT
NM_003755.3:c.947+160_947+161insAATGTGA (EIF3G)	NP_003746.2:n.947+160_947+161insAATGTGA
NM_003755.4:c.947+160_947+161insAATGTGA (EIF3G)	NP_003746.2:n.947+160_947+161insAATGTGA
NM_002566.5:c.*580_*581insTCACATT (P2RY11) MANE Select	NP_002557.2:n.*580_*581insTCACATT
NM_003755.5:c.947+160_947+161insAATGTGA (EIF3G) MANE Select	NP_003746.2:n.947+160_947+161insAATGTGA
NM_001040664.3:c.*580_*581insTCACATT (PPAN-P2RY11)	NP_001035754.1:n.*580_*581insTCACATT
NM_001198690.2:c.*1464_*1465insTCACATT (PPAN-P2RY11)	NP_001185619.1:n.*1464_*1465insTCACATT