Canonical Allele Identifier: CA2588321424

Gene: EIF3G P2RY11 PPAN-P2RY11

Linked Data

• gnomAD v4: 19-10115337-GGAAAAAAACAATAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115338_10115351del , CM000681.2:g.10115338_10115351del	GRCh38
NC_000019.9:g.10226014_10226027del , CM000681.1:g.10226014_10226027del	GRCh37
NC_000019.8:g.10087014_10087027del	NCBI36
NG_047007.1:g.8818_8831del
NG_051197.1:g.9574_9587del

Transcript Alleles

HGVS	Amino-acid change
ENST00000253108.9:c.947+128_947+141del (EIF3G) MANE Select	ENSP00000253108.3:n.947+128_947+141del
ENST00000321826.5:c.*600_*613del (P2RY11) MANE Select	ENSP00000323872.4:n.*600_*613del
ENST00000253108.8:c.947+128_947+141del (EIF3G)	ENSP00000253108.3:n.947+128_947+141del
ENST00000321826.4:c.*600_*613del (P2RY11)	ENSP00000323872.4:n.*600_*613del
ENST00000590158.1:n.966+128_966+141del (EIF3G)
ENST00000593054.5:c.341+128_341+141del (EIF3G)	ENSP00000467187.1:n.341+128_341+141del
NM_001040664.2:c.*600_*613del (PPAN-P2RY11)	NP_001035754.1:n.*600_*613del
NM_001198690.1:c.*1484_*1497del (PPAN-P2RY11)	NP_001185619.1:n.*1484_*1497del
NM_002566.4:c.*600_*613del (P2RY11)	NP_002557.2:n.*600_*613del
NM_003755.3:c.947+128_947+141del (EIF3G)	NP_003746.2:n.947+128_947+141del
NM_003755.4:c.947+128_947+141del (EIF3G)	NP_003746.2:n.947+128_947+141del
NM_002566.5:c.*600_*613del (P2RY11) MANE Select	NP_002557.2:n.*600_*613del
NM_003755.5:c.947+128_947+141del (EIF3G) MANE Select	NP_003746.2:n.947+128_947+141del
NM_001040664.3:c.*600_*613del (PPAN-P2RY11)	NP_001035754.1:n.*600_*613del
NM_001198690.2:c.*1484_*1497del (PPAN-P2RY11)	NP_001185619.1:n.*1484_*1497del