Canonical Allele Identifier: CA2171582684
Community Standard Title: NM_001013703.4(EIF2AK4):c.4065+1G=
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40017243G= , CM000677.2:g.40017243G= GRCh38
NC_000015.9:g.40309444G= , CM000677.1:g.40309444G= GRCh37
NC_000015.8:g.38096736G= NCBI36
NG_034053.1:g.88120G=

Transcript Alleles

HGVS Amino-acid Change
NM_001013703.4:c.4065+1G= MANE Select NP_001013725.2:n.4065+1G=
ENST00000263791.10:c.4065+1G= MANE Select ENSP00000263791.5:n.4065+1G=
NM_001013703.3:c.4065+1G= NP_001013725.2:n.4065+1G=
ENST00000263791.9:c.4065+1G= ENSP00000263791.5:n.4065+1G=
ENST00000558557.1:n.1057+1G=
ENST00000558629.5:n.2982+1G=
ENST00000560855.5:c.3397+1G=
XM_005254392.1:c.4065+1G= XP_005254449.1:n.4065+1G=
XM_005254392.3:c.4065+1G= XP_005254449.1:n.4065+1G=
XM_011521599.1:c.4065+1G= XP_011519901.1:n.4065+1G=
XM_011521599.2:c.4065+1G= XP_011519901.1:n.4065+1G=
XM_011521600.1:c.3894+1G= XP_011519902.1:n.3894+1G=
XM_011521600.3:c.3894+1G= XP_011519902.1:n.3894+1G=
XM_017022219.2:c.3894+1G= XP_016877708.1:n.3894+1G=