Canonical Allele Identifier: CA2171584411
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40020943G= , CM000677.2:g.40020943G= GRCh38
NC_000015.9:g.40313144G= , CM000677.1:g.40313144G= GRCh37
NC_000015.8:g.38100436G= NCBI36
NG_034053.1:g.91820G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263791.10:c.4218G= MANE Select ENSP00000263791.5:p.Gln1406=
ENST00000263791.9:c.4218G= ENSP00000263791.5:p.Gln1406=
ENST00000558557.1:n.1210G=
ENST00000558629.5:n.3135G=
ENST00000558743.1:n.418G=
ENST00000560855.5:c.3550G=
NM_001013703.3:c.4218G= NP_001013725.2:p.Gln1406=
XM_005254392.1:c.4218G= XP_005254449.1:p.Gln1406=
XM_011521599.1:c.4218G= XP_011519901.1:p.Gln1406=
XM_011521600.1:c.4047G= XP_011519902.1:p.Gln1349=
XM_005254392.3:c.4218G= XP_005254449.1:p.Gln1406=
XM_011521599.2:c.4218G= XP_011519901.1:p.Gln1406=
XM_011521600.3:c.4047G= XP_011519902.1:p.Gln1349=
XM_017022219.2:c.4047G= XP_016877708.1:p.Gln1349=
NM_001013703.4:c.4218G= MANE Select NP_001013725.2:p.Gln1406=