Canonical Allele Identifier: CA783165619

Gene: EIF3G P2RY11 PPAN-P2RY11

Linked Data

• dbSNP Id: rs1168667766
• gnomAD v4: 19-10115018-G-A
• MyVariant Identifiers: chr19:g.10225694G>A (hg19) ; chr19:g.10115018G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115018G>A , CM000681.2:g.10115018G>A	GRCh38
NC_000019.9:g.10225694G>A , CM000681.1:g.10225694G>A	GRCh37
NC_000019.8:g.10086694G>A	NCBI36
NG_047007.1:g.8498G>A
NG_051197.1:g.9907C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.*96C>T (EIF3G) MANE Select	ENSP00000253108.3:n.*96C>T
ENST00000321826.5:c.*280G>A (P2RY11) MANE Select	ENSP00000323872.4:n.*280G>A
ENST00000253108.8:c.*96C>T (EIF3G)	ENSP00000253108.3:n.*96C>T
ENST00000321826.4:c.*280G>A (P2RY11)	ENSP00000323872.4:n.*280G>A
ENST00000593054.5:c.453C>T (EIF3G)	ENSP00000467187.1:n.453C>T
NM_001040664.2:c.*280G>A (PPAN-P2RY11)	NP_001035754.1:n.*280G>A
NM_001198690.1:c.*1164G>A (PPAN-P2RY11)	NP_001185619.1:n.*1164G>A
NM_002566.4:c.*280G>A (P2RY11)	NP_002557.2:n.*280G>A
NM_003755.3:c.*96C>T (EIF3G)	NP_003746.2:n.*96C>T
NM_003755.4:c.*96C>T (EIF3G)	NP_003746.2:n.*96C>T
NM_002566.5:c.*280G>A (P2RY11) MANE Select	NP_002557.2:n.*280G>A
NM_003755.5:c.*96C>T (EIF3G) MANE Select	NP_003746.2:n.*96C>T
NM_001040664.3:c.*280G>A (PPAN-P2RY11)	NP_001035754.1:n.*280G>A
NM_001198690.2:c.*1164G>A (PPAN-P2RY11)	NP_001185619.1:n.*1164G>A