Canonical Allele Identifier: CA2405337993
Gene: ATF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39520622_39520625dup , CM000684.2:g.39520622_39520625dup GRCh38
NC_000022.10:g.39916627_39916630dup , CM000684.1:g.39916627_39916630dup GRCh37
NC_000022.9:g.38246573_38246576dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674920.3:c.-222_-219dup MANE Select ENSP00000501863.1:n.-222_-219dup
ENST00000396680.3:c.-318_-315dup ENSP00000379912.1:n.-318_-315dup
ENST00000674568.2:c.-144_-141dup ENSP00000501783.2:n.-144_-141dup
ENST00000674835.2:c.-201_-198dup ENSP00000502610.2:n.-201_-198dup
ENST00000674920.2:c.-222_-219dup ENSP00000501863.1:n.-222_-219dup
ENST00000675582.2:c.-222_-219dup ENSP00000502056.2:n.-222_-219dup
ENST00000676346.2:c.-204_-201dup ENSP00000502400.2:n.-204_-201dup
ENST00000679776.1:c.-123_-120dup ENSP00000505360.1:n.-123_-120dup
ENST00000680446.1:c.-156_-153dup ENSP00000506657.1:n.-156_-153dup
ENST00000680748.1:c.-222_-219dup ENSP00000506141.1:n.-222_-219dup
ENST00000337304.2:c.-824_-821dup ENSP00000336790.2:n.-824_-821dup
ENST00000396680.2:c.-222_-219dup ENSP00000379912.1:n.-222_-219dup
ENST00000404241.6:c.-222_-219dup ENSP00000384587.2:n.-222_-219dup
NM_001675.4:c.-824_-821dup NP_001666.2:n.-824_-821dup
NM_182810.2:c.-222_-219dup NP_877962.1:n.-222_-219dup
XM_017028807.2:c.-222_-219dup XP_016884296.1:n.-222_-219dup
NM_182810.3:c.-222_-219dup MANE Select NP_877962.1:n.-222_-219dup