Canonical Allele Identifier: CA2839576621

Gene: EIF3G P2RY11 PPAN-P2RY11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115226G>T , CM000681.2:g.10115226G>T	GRCh38
NC_000019.9:g.10225902G>T , CM000681.1:g.10225902G>T	GRCh37
NC_000019.8:g.10086902G>T	NCBI36
NG_047007.1:g.8706G>T
NG_051197.1:g.9699C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.948-97C>A (EIF3G) MANE Select	ENSP00000253108.3:n.948-97C>A
ENST00000321826.5:c.*488G>T (P2RY11) MANE Select	ENSP00000323872.4:n.*488G>T
ENST00000253108.8:c.948-97C>A (EIF3G)	ENSP00000253108.3:n.948-97C>A
ENST00000321826.4:c.*488G>T (P2RY11)	ENSP00000323872.4:n.*488G>T
ENST00000590158.1:n.967-97C>A (EIF3G)
ENST00000593054.5:c.342-97C>A (EIF3G)	ENSP00000467187.1:n.342-97C>A
NM_001040664.2:c.*488G>T (PPAN-P2RY11)	NP_001035754.1:n.*488G>T
NM_001198690.1:c.*1372G>T (PPAN-P2RY11)	NP_001185619.1:n.*1372G>T
NM_002566.4:c.*488G>T (P2RY11)	NP_002557.2:n.*488G>T
NM_003755.3:c.948-97C>A (EIF3G)	NP_003746.2:n.948-97C>A
NM_003755.4:c.948-97C>A (EIF3G)	NP_003746.2:n.948-97C>A
NM_002566.5:c.*488G>T (P2RY11) MANE Select	NP_002557.2:n.*488G>T
NM_003755.5:c.948-97C>A (EIF3G) MANE Select	NP_003746.2:n.948-97C>A
NM_001040664.3:c.*488G>T (PPAN-P2RY11)	NP_001035754.1:n.*488G>T
NM_001198690.2:c.*1372G>T (PPAN-P2RY11)	NP_001185619.1:n.*1372G>T