Canonical Allele Identifier: CA2171560999
Community Standard Title: NM_001013703.4(EIF2AK4):c.860-1G=
Gene: EIF2AK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39965685G= , CM000677.2:g.39965685G= GRCh38
NC_000015.9:g.40257886G= , CM000677.1:g.40257886G= GRCh37
NC_000015.8:g.38045178G= NCBI36
NG_034053.1:g.36562G=

Transcript Alleles

HGVS Amino-acid Change
NM_001013703.4:c.860-1G= MANE Select NP_001013725.2:n.860-1G=
ENST00000263791.10:c.860-1G= MANE Select ENSP00000263791.5:n.860-1G=
NM_001013703.3:c.860-1G= NP_001013725.2:n.860-1G=
ENST00000263791.9:c.860-1G= ENSP00000263791.5:n.860-1G=
ENST00000559624.5:c.860-1G= ENSP00000453148.1:n.860-1G=
ENST00000560855.5:c.276-1G=
XM_005254392.1:c.860-1G= XP_005254449.1:n.860-1G=
XM_005254392.3:c.860-1G= XP_005254449.1:n.860-1G=
XM_011521599.1:c.860-1G= XP_011519901.1:n.860-1G=
XM_011521599.2:c.860-1G= XP_011519901.1:n.860-1G=
XM_011521600.1:c.860-1G= XP_011519902.1:n.860-1G=
XM_011521600.3:c.860-1G= XP_011519902.1:n.860-1G=
XM_017022219.2:c.860-1G= XP_016877708.1:n.860-1G=