Canonical Allele Identifier: CA324436301

Gene: ATF4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39520625del , CM000684.2:g.39520625del	GRCh38
NC_000022.10:g.39916630del , CM000684.1:g.39916630del	GRCh37
NC_000022.9:g.38246576del	NCBI36

Transcript Alleles

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