Canonical Allele Identifier: CA347592439

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874793G>T (hg19) ; chr2:g.88575275G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575275G>T , CM000664.2:g.88575275G>T	GRCh38
NC_000002.11:g.88874793G>T , CM000664.1:g.88874793G>T	GRCh37
NC_000002.10:g.88655908G>T	NCBI36
NG_016424.1:g.57302C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000478003.2:n.2036C>A
ENST00000682276.1:n.1653C>A
ENST00000682892.1:c.1755C>A	ENSP00000507214.1:p.Ser585Arg
ENST00000682952.1:n.1847C>A
ENST00000684455.1:c.1421C>A
ENST00000684642.1:c.1605C>A	ENSP00000507355.1:p.Ser535Arg
ENST00000684740.1:n.2386C>A
ENST00000303236.9:c.2208C>A MANE Select	ENSP00000307235.3:p.Ser736Arg
ENST00000652099.1:c.2402C>A
ENST00000652736.1:n.2084C>A
ENST00000303236.7:c.2208C>A	ENSP00000307235.3:p.Ser736Arg
ENST00000415570.1:c.1845C>A	ENSP00000412076.1:p.Ser615Arg
ENST00000419748.5:c.1755C>A	ENSP00000408325.1:p.Ser585Arg
ENST00000470706.1:n.48+86C>A
NM_001313915.1:c.1755C>A	NP_001300844.1:p.Ser585Arg
NM_004836.5:c.2208C>A	NP_004827.4:p.Ser736Arg
NM_004836.6:c.2208C>A	NP_004827.4:p.Ser736Arg
NR_110236.1:n.1412G>T
XM_005264649.3:c.1524C>A	XP_005264706.1:p.Ser508Arg
XR_939749.1:n.2487C>A
XM_017005376.2:c.1524C>A	XP_016860865.1:p.Ser508Arg
NM_004836.7:c.2208C>A MANE Select	NP_004827.4:p.Ser736Arg
NM_001313915.2:c.1755C>A	NP_001300844.1:p.Ser585Arg