Canonical Allele Identifier: CA2171584431
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40021002C= , CM000677.2:g.40021002C= GRCh38
NC_000015.9:g.40313203C= , CM000677.1:g.40313203C= GRCh37
NC_000015.8:g.38100495C= NCBI36
NG_034053.1:g.91879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.4277C= MANE Select ENSP00000263791.5:p.Ala1426=
ENST00000263791.9:c.4277C= ENSP00000263791.5:p.Ala1426=
ENST00000558557.1:n.1269C=
ENST00000558629.5:n.3194C=
ENST00000558743.1:n.477C=
ENST00000560855.5:c.3609C=
NM_001013703.3:c.4277C= NP_001013725.2:p.Ala1426=
XM_005254392.1:c.4277C= XP_005254449.1:p.Ala1426=
XM_011521599.1:c.4277C= XP_011519901.1:p.Ala1426=
XM_011521600.1:c.4106C= XP_011519902.1:p.Ala1369=
XM_005254392.3:c.4277C= XP_005254449.1:p.Ala1426=
XM_011521599.2:c.4277C= XP_011519901.1:p.Ala1426=
XM_011521600.3:c.4106C= XP_011519902.1:p.Ala1369=
XM_017022219.2:c.4106C= XP_016877708.1:p.Ala1369=
NM_001013703.4:c.4277C= MANE Select NP_001013725.2:p.Ala1426=