Canonical Allele Identifier: CA10243156

Gene: ATF4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39522318C>G , CM000684.2:g.39522318C>G	GRCh38
NC_000022.10:g.39918323C>G , CM000684.1:g.39918323C>G	GRCh37
NC_000022.9:g.38248269C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_182810.3:c.772C>G MANE Select	NP_877962.1:p.Pro258Ala
ENST00000674920.3:c.772C>G MANE Select	ENSP00000501863.1:p.Pro258Ala
NM_001675.4:c.772C>G	NP_001666.2:p.Pro258Ala
NM_182810.2:c.772C>G	NP_877962.1:p.Pro258Ala
ENST00000337304.2:c.772C>G	ENSP00000336790.2:p.Pro258Ala
ENST00000396680.2:c.772C>G	ENSP00000379912.1:p.Pro258Ala
ENST00000396680.3:c.772C>G	ENSP00000379912.1:p.Pro258Ala
ENST00000404241.6:c.772C>G	ENSP00000384587.2:p.Pro258Ala
ENST00000674568.2:c.772C>G	ENSP00000501783.2:p.Pro258Ala
ENST00000674835.2:c.772C>G	ENSP00000502610.2:p.Pro258Ala
ENST00000674920.2:c.772C>G	ENSP00000501863.1:p.Pro258Ala
ENST00000675582.2:c.685C>G	ENSP00000502056.2:p.Pro229Ala
ENST00000676346.2:c.772C>G	ENSP00000502400.2:p.Pro258Ala
ENST00000679776.1:c.772C>G	ENSP00000505360.1:p.Pro258Ala
ENST00000680446.1:c.520C>G	ENSP00000506657.1:p.Pro174Ala
XM_017028807.2:c.772C>G	XP_016884296.1:p.Pro258Ala