Canonical Allele Identifier: CA403959759

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226743C>G (hg19) ; chr19:g.10116067C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10116067C>G , CM000681.2:g.10116067C>G	GRCh38
NC_000019.9:g.10226743C>G , CM000681.1:g.10226743C>G	GRCh37
NC_000019.8:g.10087743C>G	NCBI36
NG_047007.1:g.9547C>G
NG_051197.1:g.8858G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.603G>C MANE Select	ENSP00000253108.3:p.Glu201Asp
ENST00000253108.8:c.603G>C	ENSP00000253108.3:p.Glu201Asp
ENST00000587146.5:c.498G>C	ENSP00000468159.1:p.Glu166Asp
ENST00000588709.5:c.609G>C	ENSP00000465882.1:p.Glu203Asp
ENST00000589009.5:n.1505G>C
ENST00000589454.5:c.579G>C	ENSP00000466860.1:p.Glu193Asp
ENST00000590158.1:n.622G>C
ENST00000593054.5:c.36G>C	ENSP00000467187.1:p.Glu12Asp
NM_003755.3:c.603G>C	NP_003746.2:p.Glu201Asp
NM_003755.4:c.603G>C	NP_003746.2:p.Glu201Asp
NM_003755.5:c.603G>C MANE Select	NP_003746.2:p.Glu201Asp