Canonical Allele Identifier: CA324437274

Gene: ATF4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39521910C>T , CM000684.2:g.39521910C>T	GRCh38
NC_000022.10:g.39917915C>T , CM000684.1:g.39917915C>T	GRCh37
NC_000022.9:g.38247861C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_182810.3:c.364C>T MANE Select	NP_877962.1:p.Leu122Phe
ENST00000674920.3:c.364C>T MANE Select	ENSP00000501863.1:p.Leu122Phe
NM_001675.4:c.364C>T	NP_001666.2:p.Leu122Phe
NM_182810.2:c.364C>T	NP_877962.1:p.Leu122Phe
ENST00000337304.2:c.364C>T	ENSP00000336790.2:p.Leu122Phe
ENST00000396680.2:c.364C>T	ENSP00000379912.1:p.Leu122Phe
ENST00000396680.3:c.364C>T	ENSP00000379912.1:p.Leu122Phe
ENST00000404241.6:c.364C>T	ENSP00000384587.2:p.Leu122Phe
ENST00000674568.2:c.364C>T	ENSP00000501783.2:p.Leu122Phe
ENST00000674835.2:c.364C>T	ENSP00000502610.2:p.Leu122Phe
ENST00000674920.2:c.364C>T	ENSP00000501863.1:p.Leu122Phe
ENST00000675582.2:c.277C>T	ENSP00000502056.2:p.Leu93Phe
ENST00000676346.2:c.364C>T	ENSP00000502400.2:p.Leu122Phe
ENST00000679776.1:c.364C>T	ENSP00000505360.1:p.Leu122Phe
ENST00000680446.1:c.112C>T	ENSP00000506657.1:p.Leu38Phe
ENST00000680748.1:c.*171C>T	ENSP00000506141.1:n.*171C>T
XM_017028807.2:c.364C>T	XP_016884296.1:p.Leu122Phe