Canonical Allele Identifier: CA2813565526
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115316_10115317insT , CM000681.2:g.10115316_10115317insT GRCh38
NC_000019.9:g.10225992_10225993insT , CM000681.1:g.10225992_10225993insT GRCh37
NC_000019.8:g.10086992_10086993insT NCBI36
NG_047007.1:g.8796_8797insT
NG_051197.1:g.9608_9609insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+162_947+163insA (EIF3G) MANE Select ENSP00000253108.3:n.947+162_947+163insA
ENST00000321826.5:c.*578_*579insT (P2RY11) MANE Select ENSP00000323872.4:n.*578_*579insT
ENST00000253108.8:c.947+162_947+163insA (EIF3G) ENSP00000253108.3:n.947+162_947+163insA
ENST00000321826.4:c.*578_*579insT (P2RY11) ENSP00000323872.4:n.*578_*579insT
ENST00000590158.1:n.966+162_966+163insA (EIF3G)
ENST00000593054.5:c.341+162_341+163insA (EIF3G) ENSP00000467187.1:n.341+162_341+163insA
NM_001040664.2:c.*578_*579insT (PPAN-P2RY11) NP_001035754.1:n.*578_*579insT
NM_001198690.1:c.*1462_*1463insT (PPAN-P2RY11) NP_001185619.1:n.*1462_*1463insT
NM_002566.4:c.*578_*579insT (P2RY11) NP_002557.2:n.*578_*579insT
NM_003755.3:c.947+162_947+163insA (EIF3G) NP_003746.2:n.947+162_947+163insA
NM_003755.4:c.947+162_947+163insA (EIF3G) NP_003746.2:n.947+162_947+163insA
NM_002566.5:c.*578_*579insT (P2RY11) MANE Select NP_002557.2:n.*578_*579insT
NM_003755.5:c.947+162_947+163insA (EIF3G) MANE Select NP_003746.2:n.947+162_947+163insA
NM_001040664.3:c.*578_*579insT (PPAN-P2RY11) NP_001035754.1:n.*578_*579insT
NM_001198690.2:c.*1462_*1463insT (PPAN-P2RY11) NP_001185619.1:n.*1462_*1463insT
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