Canonical Allele Identifier: CA391676946

Gene: EIF2AK4

Linked Data

• MyVariant Identifiers: chr15:g.40313139G>A (hg19) ; chr15:g.40020938G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40020938G>A , CM000677.2:g.40020938G>A	GRCh38
NC_000015.9:g.40313139G>A , CM000677.1:g.40313139G>A	GRCh37
NC_000015.8:g.38100431G>A	NCBI36
NG_034053.1:g.91815G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263791.10:c.4213G>A MANE Select	ENSP00000263791.5:p.Gly1405Ser
ENST00000263791.9:c.4213G>A	ENSP00000263791.5:p.Gly1405Ser
ENST00000558557.1:n.1205G>A
ENST00000558629.5:n.3130G>A
ENST00000558743.1:n.413G>A
ENST00000560855.5:c.3545G>A
NM_001013703.3:c.4213G>A	NP_001013725.2:p.Gly1405Ser
XM_005254392.1:c.4213G>A	XP_005254449.1:p.Gly1405Ser
XM_011521599.1:c.4213G>A	XP_011519901.1:p.Gly1405Ser
XM_011521600.1:c.4042G>A	XP_011519902.1:p.Gly1348Ser
XM_005254392.3:c.4213G>A	XP_005254449.1:p.Gly1405Ser
XM_011521599.2:c.4213G>A	XP_011519901.1:p.Gly1405Ser
XM_011521600.3:c.4042G>A	XP_011519902.1:p.Gly1348Ser
XM_017022219.2:c.4042G>A	XP_016877708.1:p.Gly1348Ser
NM_001013703.4:c.4213G>A MANE Select	NP_001013725.2:p.Gly1405Ser