Canonical Allele Identifier: CA631709098

Gene: EIF3G

Linked Data

• dbSNP Id: rs1264687629
• gnomAD v2: 19-10226330-CAG-C
• MyVariant Identifiers: chr19:g.10226331_10226332del (hg19) ; chr19:g.10115655_10115656del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115655_10115656del , CM000681.2:g.10115655_10115656del	GRCh38
NC_000019.9:g.10226331_10226332del , CM000681.1:g.10226331_10226332del	GRCh37
NC_000019.8:g.10087331_10087332del	NCBI36
NG_047007.1:g.9135_9136del
NG_051197.1:g.9269_9270del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.840+28_840+29del MANE Select	ENSP00000253108.3:n.840+28_840+29del
ENST00000253108.8:c.840+28_840+29del	ENSP00000253108.3:n.840+28_840+29del
ENST00000589454.5:c.816+28_816+29del	ENSP00000466860.1:n.816+28_816+29del
ENST00000590158.1:n.859+28_859+29del
ENST00000593054.5:c.234+28_234+29del	ENSP00000467187.1:n.234+28_234+29del
NM_003755.3:c.840+28_840+29del	NP_003746.2:n.840+28_840+29del
NM_003755.4:c.840+28_840+29del	NP_003746.2:n.840+28_840+29del
NM_003755.5:c.840+28_840+29del MANE Select	NP_003746.2:n.840+28_840+29del