Canonical Allele Identifier: CA489702440

Gene: EIF2AK4

Linked Data

• MyVariant Identifiers: chr15:g.40308726T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40016525T>A , CM000677.2:g.40016525T>A	GRCh38
NC_000015.9:g.40308726T>A , CM000677.1:g.40308726T>A	GRCh37
NC_000015.8:g.38096018T>A	NCBI36
NG_034053.1:g.87402T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263791.10:c.3783T>A MANE Select	ENSP00000263791.5:p.Ile1261=
ENST00000263791.9:c.3783T>A	ENSP00000263791.5:p.Ile1261=
ENST00000558557.1:n.923-583T>A
ENST00000558629.5:n.2700T>A
ENST00000560855.5:c.3115T>A
NM_001013703.3:c.3783T>A	NP_001013725.2:p.Ile1261=
XM_005254392.1:c.3783T>A	XP_005254449.1:p.Ile1261=
XM_011521599.1:c.3783T>A	XP_011519901.1:p.Ile1261=
XM_011521600.1:c.3760-583T>A	XP_011519902.1:n.3760-583T>A
XM_005254392.3:c.3783T>A	XP_005254449.1:p.Ile1261=
XM_011521599.2:c.3783T>A	XP_011519901.1:p.Ile1261=
XM_011521600.3:c.3760-583T>A	XP_011519902.1:n.3760-583T>A
XM_017022219.2:c.3760-583T>A	XP_016877708.1:n.3760-583T>A
NM_001013703.4:c.3783T>A MANE Select	NP_001013725.2:p.Ile1261=