Canonical Allele Identifier: CA514786234
Gene: ATF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39522458G>A , CM000684.2:g.39522458G>A GRCh38
NC_000022.10:g.39918463G>A , CM000684.1:g.39918463G>A GRCh37
NC_000022.9:g.38248409G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674920.3:c.912G>A MANE Select ENSP00000501863.1:p.Glu304=
ENST00000396680.3:c.912G>A ENSP00000379912.1:p.Glu304=
ENST00000674568.2:c.912G>A ENSP00000501783.2:p.Glu304=
ENST00000674835.2:c.912G>A ENSP00000502610.2:p.Glu304=
ENST00000674920.2:c.912G>A ENSP00000501863.1:p.Glu304=
ENST00000675582.2:c.825G>A ENSP00000502056.2:p.Glu275=
ENST00000676346.2:c.912G>A ENSP00000502400.2:p.Glu304=
ENST00000679776.1:c.912G>A ENSP00000505360.1:p.Glu304=
ENST00000680446.1:c.660G>A ENSP00000506657.1:p.Glu220=
ENST00000337304.2:c.912G>A ENSP00000336790.2:p.Glu304=
ENST00000396680.2:c.912G>A ENSP00000379912.1:p.Glu304=
ENST00000404241.6:c.912G>A ENSP00000384587.2:p.Glu304=
NM_001675.4:c.912G>A NP_001666.2:p.Glu304=
NM_182810.2:c.912G>A NP_877962.1:p.Glu304=
XM_017028807.2:c.912G>A XP_016884296.1:p.Glu304=
NM_182810.3:c.912G>A MANE Select NP_877962.1:p.Glu304=