Canonical Allele Identifier: CA2171566205
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39978117T= , CM000677.2:g.39978117T= GRCh38
NC_000015.9:g.40270318T= , CM000677.1:g.40270318T= GRCh37
NC_000015.8:g.38057610T= NCBI36
NG_034053.1:g.48994T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263791.10:c.2289T= MANE Select ENSP00000263791.5:p.Asn763=
ENST00000263791.9:c.2289T= ENSP00000263791.5:p.Asn763=
ENST00000560855.5:c.1705T=
ENST00000624709.1:n.1139T=
NM_001013703.3:c.2289T= NP_001013725.2:p.Asn763=
XM_005254392.1:c.2289T= XP_005254449.1:p.Asn763=
XM_011521599.1:c.2289T= XP_011519901.1:p.Asn763=
XM_011521600.1:c.2289T= XP_011519902.1:p.Asn763=
XM_005254392.3:c.2289T= XP_005254449.1:p.Asn763=
XM_011521599.2:c.2289T= XP_011519901.1:p.Asn763=
XM_011521600.3:c.2289T= XP_011519902.1:p.Asn763=
XM_017022219.2:c.2289T= XP_016877708.1:p.Asn763=
NM_001013703.4:c.2289T= MANE Select NP_001013725.2:p.Asn763=