Canonical Allele Identifier: CA9186824
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs772114181
ExAC: 19:10226293 GCTAGGACAGGCGACC / G
gnomAD v2: 19-10226293-GCTAGGACAGGCGACC-G
gnomAD v3: 19-10115617-GCTAGGACAGGCGACC-G
gnomAD v4: 19-10115617-GCTAGGACAGGCGACC-G
MyVariant Identifiers: chr19:g.10226294_10226308del (hg19) chr19:g.10115618_10115632del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115626_10115640del , CM000681.2:g.10115626_10115640del GRCh38
NC_000019.9:g.10226302_10226316del , CM000681.1:g.10226302_10226316del GRCh37
NC_000019.8:g.10087302_10087316del NCBI36
NG_047007.1:g.9106_9120del
NG_051197.1:g.9293_9307del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.841-47_841-33del MANE Select ENSP00000253108.3:n.841-47_841-33del
ENST00000253108.8:c.841-47_841-33del ENSP00000253108.3:n.841-47_841-33del
ENST00000589454.5:c.817-47_817-33del ENSP00000466860.1:n.817-47_817-33del
ENST00000590158.1:n.860-47_860-33del
ENST00000593054.5:c.235-47_235-33del ENSP00000467187.1:n.235-47_235-33del
NM_003755.3:c.841-47_841-33del NP_003746.2:n.841-47_841-33del
NM_003755.4:c.841-47_841-33del NP_003746.2:n.841-47_841-33del
NM_003755.5:c.841-47_841-33del MANE Select NP_003746.2:n.841-47_841-33del
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