Canonical Allele Identifier: CA437398128

Gene: EIF4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186783859T>G , CM000665.2:g.186783859T>G	GRCh38
NC_000003.11:g.186501648T>G , CM000665.1:g.186501648T>G	GRCh37
NC_000003.10:g.187984342T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001967.4:c.29+220T>G MANE Select	NP_001958.2:n.29+220T>G
ENST00000323963.10:c.29+220T>G MANE Select	ENSP00000326381.5:n.29+220T>G
NM_001967.3:c.29+220T>G	NP_001958.2:n.29+220T>G
ENST00000323963.9:c.29+220T>G	ENSP00000326381.5:n.29+220T>G
ENST00000425053.5:c.29+220T>G	ENSP00000413529.1:n.29+220T>G
ENST00000426808.5:c.29+220T>G	ENSP00000392686.1:n.29+220T>G
ENST00000429589.5:c.29+220T>G	ENSP00000388237.1:n.29+220T>G
ENST00000440191.6:c.29+220T>G	ENSP00000398370.2:n.29+220T>G
ENST00000441007.5:c.29+220T>G	ENSP00000407504.1:n.29+220T>G
ENST00000443963.5:c.29+220T>G	ENSP00000402313.1:n.29+220T>G
ENST00000445596.5:c.29+220T>G	ENSP00000415878.1:n.29+220T>G
ENST00000465032.5:n.63+220T>G
ENST00000465222.1:n.65+220T>G
ENST00000465267.5:n.63+220T>G
ENST00000475653.5:n.47+220T>G
ENST00000485101.5:n.62+220T>G
ENST00000486805.5:n.63+220T>G
ENST00000491473.5:n.63+220T>G
ENST00000495049.5:n.63+220T>G