Canonical Allele Identifier: CA403957928

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226242A>T (hg19) ; chr19:g.10115566A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115566A>T , CM000681.2:g.10115566A>T	GRCh38
NC_000019.9:g.10226242A>T , CM000681.1:g.10226242A>T	GRCh37
NC_000019.8:g.10087242A>T	NCBI36
NG_047007.1:g.9046A>T
NG_051197.1:g.9359T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.860T>A MANE Select	ENSP00000253108.3:p.Phe287Tyr
ENST00000253108.8:c.860T>A	ENSP00000253108.3:p.Phe287Tyr
ENST00000589454.5:c.836T>A	ENSP00000466860.1:p.Phe279Tyr
ENST00000590158.1:n.879T>A
ENST00000593054.5:c.254T>A	ENSP00000467187.1:p.Phe85Tyr
NM_003755.3:c.860T>A	NP_003746.2:p.Phe287Tyr
NM_003755.4:c.860T>A	NP_003746.2:p.Phe287Tyr
NM_003755.5:c.860T>A MANE Select	NP_003746.2:p.Phe287Tyr