Canonical Allele Identifier: CA631709097

Gene: EIF3G

Linked Data

• dbSNP Id: rs1192316947
• gnomAD v2: 19-10226316-A-AAGTGACCCTCACAC
• gnomAD v3: 19-10115640-A-AAGTGACCCTCACAC
• gnomAD v4: 19-10115640-A-AAGTGACCCTCACAC
• MyVariant Identifiers: chr19:g.10226316_10226317insAGTGACCCTCACAC (hg19) ; chr19:g.10115640_10115641insAGTGACCCTCACAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115643_10115656dup , CM000681.2:g.10115643_10115656dup	GRCh38
NC_000019.9:g.10226319_10226332dup , CM000681.1:g.10226319_10226332dup	GRCh37
NC_000019.8:g.10087319_10087332dup	NCBI36
NG_047007.1:g.9123_9136dup
NG_051197.1:g.9271_9284dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.840+30_840+43dup MANE Select	ENSP00000253108.3:n.840+30_840+43dup
ENST00000253108.8:c.840+30_840+43dup	ENSP00000253108.3:n.840+30_840+43dup
ENST00000589454.5:c.816+30_816+43dup	ENSP00000466860.1:n.816+30_816+43dup
ENST00000590158.1:n.859+30_859+43dup
ENST00000593054.5:c.234+30_234+43dup	ENSP00000467187.1:n.234+30_234+43dup
NM_003755.3:c.840+30_840+43dup	NP_003746.2:n.840+30_840+43dup
NM_003755.4:c.840+30_840+43dup	NP_003746.2:n.840+30_840+43dup
NM_003755.5:c.840+30_840+43dup MANE Select	NP_003746.2:n.840+30_840+43dup