Canonical Allele Identifier: CA993413563
Gene: EIF3G HGNC NCBI
P2RY11 HGNC NCBI
PPAN-P2RY11 HGNC NCBI

Linked Data

dbSNP Id: rs2089222458

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115317C>T , CM000681.2:g.10115317C>T GRCh38
NC_000019.9:g.10225993C>T , CM000681.1:g.10225993C>T GRCh37
NC_000019.8:g.10086993C>T NCBI36
NG_047007.1:g.8797C>T
NG_051197.1:g.9608G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+162G>A (EIF3G) MANE Select ENSP00000253108.3:n.947+162G>A
ENST00000321826.5:c.*579C>T (P2RY11) MANE Select ENSP00000323872.4:n.*579C>T
ENST00000253108.8:c.947+162G>A (EIF3G) ENSP00000253108.3:n.947+162G>A
ENST00000321826.4:c.*579C>T (P2RY11) ENSP00000323872.4:n.*579C>T
ENST00000590158.1:n.966+162G>A (EIF3G)
ENST00000593054.5:c.341+162G>A (EIF3G) ENSP00000467187.1:n.341+162G>A
NM_001040664.2:c.*579C>T (PPAN-P2RY11) NP_001035754.1:n.*579C>T
NM_001198690.1:c.*1463C>T (PPAN-P2RY11) NP_001185619.1:n.*1463C>T
NM_002566.4:c.*579C>T (P2RY11) NP_002557.2:n.*579C>T
NM_003755.3:c.947+162G>A (EIF3G) NP_003746.2:n.947+162G>A
NM_003755.4:c.947+162G>A (EIF3G) NP_003746.2:n.947+162G>A
NM_002566.5:c.*579C>T (P2RY11) MANE Select NP_002557.2:n.*579C>T
NM_003755.5:c.947+162G>A (EIF3G) MANE Select NP_003746.2:n.947+162G>A
NM_001040664.3:c.*579C>T (PPAN-P2RY11) NP_001035754.1:n.*579C>T
NM_001198690.2:c.*1463C>T (PPAN-P2RY11) NP_001185619.1:n.*1463C>T