Canonical Allele Identifier: CA993413600

Gene: EIF3G PPAN-P2RY11 P2RY11

Linked Data

• dbSNP Id: rs2089224333
• gnomAD v3: 19-10115377-G-C
• gnomAD v4: 19-10115377-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115377G>C , CM000681.2:g.10115377G>C	GRCh38
NC_000019.9:g.10226053G>C , CM000681.1:g.10226053G>C	GRCh37
NC_000019.8:g.10087053G>C	NCBI36
NG_047007.1:g.8857G>C
NG_051197.1:g.9548C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000253108.9:c.947+102C>G (EIF3G) MANE Select	ENSP00000253108.3:n.947+102C>G
ENST00000253108.8:c.947+102C>G (EIF3G)	ENSP00000253108.3:n.947+102C>G
ENST00000590158.1:n.966+102C>G (EIF3G)
ENST00000593054.5:c.341+102C>G (EIF3G)	ENSP00000467187.1:n.341+102C>G
NM_001040664.2:c.*639G>C (PPAN-P2RY11)	NP_001035754.1:n.*639G>C
NM_001198690.1:c.*1523G>C (PPAN-P2RY11)	NP_001185619.1:n.*1523G>C
NM_002566.4:c.*639G>C (P2RY11)	NP_002557.2:n.*639G>C
NM_003755.3:c.947+102C>G (EIF3G)	NP_003746.2:n.947+102C>G
NM_003755.4:c.947+102C>G (EIF3G)	NP_003746.2:n.947+102C>G
NM_003755.5:c.947+102C>G (EIF3G) MANE Select	NP_003746.2:n.947+102C>G