Canonical Allele Identifier: CA2588321267
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

gnomAD v4: 19-10115194-G-GA
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115194_10115195insA , CM000681.2:g.10115194_10115195insA GRCh38
NC_000019.9:g.10225870_10225871insA , CM000681.1:g.10225870_10225871insA GRCh37
NC_000019.8:g.10086870_10086871insA NCBI36
NG_047007.1:g.8674_8675insA
NG_051197.1:g.9730_9731insT

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.948-66_948-65insT (EIF3G) MANE Select ENSP00000253108.3:n.948-66_948-65insT
ENST00000321826.5:c.*456_*457insA (P2RY11) MANE Select ENSP00000323872.4:n.*456_*457insA
ENST00000253108.8:c.948-66_948-65insT (EIF3G) ENSP00000253108.3:n.948-66_948-65insT
ENST00000321826.4:c.*456_*457insA (P2RY11) ENSP00000323872.4:n.*456_*457insA
ENST00000590158.1:n.967-66_967-65insT (EIF3G)
ENST00000593054.5:c.342-66_342-65insT (EIF3G) ENSP00000467187.1:n.342-66_342-65insT
NM_001040664.2:c.*456_*457insA (PPAN-P2RY11) NP_001035754.1:n.*456_*457insA
NM_001198690.1:c.*1340_*1341insA (PPAN-P2RY11) NP_001185619.1:n.*1340_*1341insA
NM_002566.4:c.*456_*457insA (P2RY11) NP_002557.2:n.*456_*457insA
NM_003755.3:c.948-66_948-65insT (EIF3G) NP_003746.2:n.948-66_948-65insT
NM_003755.4:c.948-66_948-65insT (EIF3G) NP_003746.2:n.948-66_948-65insT
NM_002566.5:c.*456_*457insA (P2RY11) MANE Select NP_002557.2:n.*456_*457insA
NM_003755.5:c.948-66_948-65insT (EIF3G) MANE Select NP_003746.2:n.948-66_948-65insT
NM_001040664.3:c.*456_*457insA (PPAN-P2RY11) NP_001035754.1:n.*456_*457insA
NM_001198690.2:c.*1340_*1341insA (PPAN-P2RY11) NP_001185619.1:n.*1340_*1341insA
Search 100 bp 5'
Search 100 bp 3'