Canonical Allele Identifier: CA2588321492
Gene: EIF3G HGNC NCBI
PPAN-P2RY11 HGNC NCBI
P2RY11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115382_10115383del , CM000681.2:g.10115382_10115383del GRCh38
NC_000019.9:g.10226058_10226059del , CM000681.1:g.10226058_10226059del GRCh37
NC_000019.8:g.10087058_10087059del NCBI36
NG_047007.1:g.8862_8863del
NG_051197.1:g.9542_9543del

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+96_947+97del (EIF3G) MANE Select ENSP00000253108.3:n.947+96_947+97del
ENST00000253108.8:c.947+96_947+97del (EIF3G) ENSP00000253108.3:n.947+96_947+97del
ENST00000590158.1:n.966+96_966+97del (EIF3G)
ENST00000593054.5:c.341+96_341+97del (EIF3G) ENSP00000467187.1:n.341+96_341+97del
NM_001040664.2:c.*644_*645del (PPAN-P2RY11) NP_001035754.1:n.*644_*645del
NM_001198690.1:c.*1528_*1529del (PPAN-P2RY11) NP_001185619.1:n.*1528_*1529del
NM_002566.4:c.*644_*645del (P2RY11) NP_002557.2:n.*644_*645del
NM_003755.3:c.947+96_947+97del (EIF3G) NP_003746.2:n.947+96_947+97del
NM_003755.4:c.947+96_947+97del (EIF3G) NP_003746.2:n.947+96_947+97del
NM_003755.5:c.947+96_947+97del (EIF3G) MANE Select NP_003746.2:n.947+96_947+97del