Canonical Allele Identifier: CA411623010

Gene: ATF4

Linked Data

• dbSNP Id: rs4894
• gnomAD v4: 22-39521510-A-T
• MyVariant Identifiers: chr22:g.39917515A>T (hg19) ; chr22:g.39521510A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39521510A>T , CM000684.2:g.39521510A>T	GRCh38
NC_000022.10:g.39917515A>T , CM000684.1:g.39917515A>T	GRCh37
NC_000022.9:g.38247461A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000674920.3:c.65A>T MANE Select	ENSP00000501863.1:p.Gln22Leu
ENST00000396680.3:c.65A>T	ENSP00000379912.1:p.Gln22Leu
ENST00000674568.2:c.65A>T	ENSP00000501783.2:p.Gln22Leu
ENST00000674835.2:c.65A>T	ENSP00000502610.2:p.Gln22Leu
ENST00000674920.2:c.65A>T	ENSP00000501863.1:p.Gln22Leu
ENST00000675582.2:c.30+35A>T	ENSP00000502056.2:n.30+35A>T
ENST00000676346.2:c.65A>T	ENSP00000502400.2:p.Gln22Leu
ENST00000676430.1:c.162A>T	ENSP00000501638.1:p.Pro54=
ENST00000679776.1:c.65A>T	ENSP00000505360.1:p.Gln22Leu
ENST00000680446.1:c.-26-263A>T	ENSP00000506657.1:n.-26-263A>T
ENST00000680748.1:c.65A>T	ENSP00000506141.1:p.Gln22Leu
ENST00000337304.2:c.65A>T	ENSP00000336790.2:p.Gln22Leu
ENST00000396680.2:c.65A>T	ENSP00000379912.1:p.Gln22Leu
ENST00000404241.6:c.65A>T	ENSP00000384587.2:p.Gln22Leu
NM_001675.4:c.65A>T	NP_001666.2:p.Gln22Leu
NM_182810.2:c.65A>T	NP_877962.1:p.Gln22Leu
XM_017028807.2:c.65A>T	XP_016884296.1:p.Gln22Leu
NM_182810.3:c.65A>T MANE Select	NP_877962.1:p.Gln22Leu