Canonical Allele Identifier: CA2813565524
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115309_10115312del , CM000681.2:g.10115309_10115312del GRCh38
NC_000019.9:g.10225985_10225988del , CM000681.1:g.10225985_10225988del GRCh37
NC_000019.8:g.10086985_10086988del NCBI36
NG_047007.1:g.8789_8792del
NG_051197.1:g.9613_9616del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+167_947+170del (EIF3G) MANE Select ENSP00000253108.3:n.947+167_947+170del
ENST00000321826.5:c.*571_*574del (P2RY11) MANE Select ENSP00000323872.4:n.*571_*574del
ENST00000253108.8:c.947+167_947+170del (EIF3G) ENSP00000253108.3:n.947+167_947+170del
ENST00000321826.4:c.*571_*574del (P2RY11) ENSP00000323872.4:n.*571_*574del
ENST00000590158.1:n.966+167_966+170del (EIF3G)
ENST00000593054.5:c.341+167_341+170del (EIF3G) ENSP00000467187.1:n.341+167_341+170del
NM_001040664.2:c.*571_*574del (PPAN-P2RY11) NP_001035754.1:n.*571_*574del
NM_001198690.1:c.*1455_*1458del (PPAN-P2RY11) NP_001185619.1:n.*1455_*1458del
NM_002566.4:c.*571_*574del (P2RY11) NP_002557.2:n.*571_*574del
NM_003755.3:c.947+167_947+170del (EIF3G) NP_003746.2:n.947+167_947+170del
NM_003755.4:c.947+167_947+170del (EIF3G) NP_003746.2:n.947+167_947+170del
NM_002566.5:c.*571_*574del (P2RY11) MANE Select NP_002557.2:n.*571_*574del
NM_003755.5:c.947+167_947+170del (EIF3G) MANE Select NP_003746.2:n.947+167_947+170del
NM_001040664.3:c.*571_*574del (PPAN-P2RY11) NP_001035754.1:n.*571_*574del
NM_001198690.2:c.*1455_*1458del (PPAN-P2RY11) NP_001185619.1:n.*1455_*1458del
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