Canonical Allele Identifier: CA2171584421
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40020974C= , CM000677.2:g.40020974C= GRCh38
NC_000015.9:g.40313175C= , CM000677.1:g.40313175C= GRCh37
NC_000015.8:g.38100467C= NCBI36
NG_034053.1:g.91851C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.4249C= MANE Select ENSP00000263791.5:p.Gln1417=
ENST00000263791.9:c.4249C= ENSP00000263791.5:p.Gln1417=
ENST00000558557.1:n.1241C=
ENST00000558629.5:n.3166C=
ENST00000558743.1:n.449C=
ENST00000560855.5:c.3581C=
NM_001013703.3:c.4249C= NP_001013725.2:p.Gln1417=
XM_005254392.1:c.4249C= XP_005254449.1:p.Gln1417=
XM_011521599.1:c.4249C= XP_011519901.1:p.Gln1417=
XM_011521600.1:c.4078C= XP_011519902.1:p.Gln1360=
XM_005254392.3:c.4249C= XP_005254449.1:p.Gln1417=
XM_011521599.2:c.4249C= XP_011519901.1:p.Gln1417=
XM_011521600.3:c.4078C= XP_011519902.1:p.Gln1360=
XM_017022219.2:c.4078C= XP_016877708.1:p.Gln1360=
NM_001013703.4:c.4249C= MANE Select NP_001013725.2:p.Gln1417=