Canonical Allele Identifier: CA2171588675
Community Standard Title: NM_001013703.4(EIF2AK4):c.4562-8G=
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40030351G= , CM000677.2:g.40030351G= GRCh38
NC_000015.9:g.40322552G= , CM000677.1:g.40322552G= GRCh37
NC_000015.8:g.38109844G= NCBI36
NG_034053.1:g.101228G=

Transcript Alleles

HGVS Amino-acid Change
NM_001013703.4:c.4562-8G= MANE Select NP_001013725.2:n.4562-8G=
ENST00000263791.10:c.4562-8G= MANE Select ENSP00000263791.5:n.4562-8G=
NM_001013703.3:c.4562-8G= NP_001013725.2:n.4562-8G=
ENST00000263791.9:c.4562-8G= ENSP00000263791.5:n.4562-8G=
ENST00000558557.1:n.1554-8G=
ENST00000558629.5:n.3479-8G=
ENST00000560855.5:c.3894-8G=
XM_005254392.1:c.4562-8G= XP_005254449.1:n.4562-8G=
XM_005254392.3:c.4562-8G= XP_005254449.1:n.4562-8G=
XM_011521599.1:c.4562-8G= XP_011519901.1:n.4562-8G=
XM_011521599.2:c.4562-8G= XP_011519901.1:n.4562-8G=
XM_011521600.1:c.4391-8G= XP_011519902.1:n.4391-8G=
XM_011521600.3:c.4391-8G= XP_011519902.1:n.4391-8G=
XM_017022219.2:c.4391-8G= XP_016877708.1:n.4391-8G=