Canonical Allele Identifier: CA10243214

Gene: ATF4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39522512G>C , CM000684.2:g.39522512G>C	GRCh38
NC_000022.10:g.39918517G>C , CM000684.1:g.39918517G>C	GRCh37
NC_000022.9:g.38248463G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_182810.3:c.966G>C MANE Select	NP_877962.1:p.Glu322Asp
ENST00000674920.3:c.966G>C MANE Select	ENSP00000501863.1:p.Glu322Asp
NM_001675.4:c.966G>C	NP_001666.2:p.Glu322Asp
NM_182810.2:c.966G>C	NP_877962.1:p.Glu322Asp
ENST00000337304.2:c.966G>C	ENSP00000336790.2:p.Glu322Asp
ENST00000396680.2:c.966G>C	ENSP00000379912.1:p.Glu322Asp
ENST00000396680.3:c.966G>C	ENSP00000379912.1:p.Glu322Asp
ENST00000404241.6:c.966G>C	ENSP00000384587.2:p.Glu322Asp
ENST00000674568.2:c.966G>C	ENSP00000501783.2:p.Glu322Asp
ENST00000674835.2:c.966G>C	ENSP00000502610.2:p.Glu322Asp
ENST00000674920.2:c.966G>C	ENSP00000501863.1:p.Glu322Asp
ENST00000675582.2:c.879G>C	ENSP00000502056.2:p.Glu293Asp
ENST00000676346.2:c.966G>C	ENSP00000502400.2:p.Glu322Asp
ENST00000679776.1:c.966G>C	ENSP00000505360.1:p.Glu322Asp
ENST00000680446.1:c.714G>C	ENSP00000506657.1:p.Glu238Asp
XM_017028807.2:c.966G>C	XP_016884296.1:p.Glu322Asp