Canonical Allele Identifier: CA391696465
Gene: EIF2AK4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40016520T>A , CM000677.2:g.40016520T>A GRCh38
NC_000015.9:g.40308721T>A , CM000677.1:g.40308721T>A GRCh37
NC_000015.8:g.38096013T>A NCBI36
NG_034053.1:g.87397T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.3778T>A MANE Select ENSP00000263791.5:p.Phe1260Ile
ENST00000263791.9:c.3778T>A ENSP00000263791.5:p.Phe1260Ile
ENST00000558557.1:n.923-588T>A
ENST00000558629.5:n.2695T>A
ENST00000560855.5:c.3110T>A
NM_001013703.3:c.3778T>A NP_001013725.2:p.Phe1260Ile
XM_005254392.1:c.3778T>A XP_005254449.1:p.Phe1260Ile
XM_011521599.1:c.3778T>A XP_011519901.1:p.Phe1260Ile
XM_011521600.1:c.3760-588T>A XP_011519902.1:n.3760-588T>A
XM_005254392.3:c.3778T>A XP_005254449.1:p.Phe1260Ile
XM_011521599.2:c.3778T>A XP_011519901.1:p.Phe1260Ile
XM_011521600.3:c.3760-588T>A XP_011519902.1:n.3760-588T>A
XM_017022219.2:c.3760-588T>A XP_016877708.1:n.3760-588T>A
NM_001013703.4:c.3778T>A MANE Select NP_001013725.2:p.Phe1260Ile