Canonical Allele Identifier: CA324436303

Gene: ATF4

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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