Canonical Allele Identifier: CA508141663

Gene: ATF5

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49930892C>G , CM000681.2:g.49930892C>G	GRCh38
NC_000019.9:g.50434149C>G , CM000681.1:g.50434149C>G	GRCh37
NC_000019.8:g.55125961C>G	NCBI36
NG_021170.1:g.3614G>C
NG_023448.1:g.3840G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001193646.2:c.42C>G MANE Select	NP_001180575.1:p.Ala14=
ENST00000423777.7:c.42C>G MANE Select	ENSP00000396954.1:p.Ala14=
NM_001193646.1:c.42C>G	NP_001180575.1:p.Ala14=
NM_001290746.1:c.42C>G	NP_001277675.1:p.Ala14=
NM_001290746.2:c.42C>G	NP_001277675.1:p.Ala14=
NM_012068.5:c.42C>G	NP_036200.2:p.Ala14=
NM_012068.6:c.42C>G	NP_036200.2:p.Ala14=
ENST00000423777.6:c.42C>G	ENSP00000396954.1:p.Ala14=
ENST00000451973.1:c.191+20999G>C	ENSP00000391489.1:n.191+20999G>C
ENST00000595125.5:c.42C>G	ENSP00000470633.1:p.Ala14=
ENST00000596658.1:c.42C>G	ENSP00000470464.1:p.Ala14=
ENST00000597227.5:c.42C>G	ENSP00000470978.1:p.Ala14=
ENST00000600336.1:c.42C>G	ENSP00000471162.1:p.Ala14=
ENST00000676286.1:c.166C>G	ENSP00000502402.1:p.Pro56Ala
XM_011526629.1:c.42C>G	XP_011524931.1:p.Ala14=
XM_011526629.3:c.42C>G	XP_011524931.1:p.Ala14=