Canonical Allele Identifier: CA1754479

Gene: EIF2AK3

Linked Data

• dbSNP Id: rs761841704
• ExAC: 2:88874754 C / T
• gnomAD v2: 2-88874754-C-T
• gnomAD v4: 2-88575236-C-T
• MyVariant Identifiers: chr2:g.88874754C>T (hg19) ; chr2:g.88575236C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575236C>T , CM000664.2:g.88575236C>T	GRCh38
NC_000002.11:g.88874754C>T , CM000664.1:g.88874754C>T	GRCh37
NC_000002.10:g.88655869C>T	NCBI36
NG_016424.1:g.57341G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2075G>A
ENST00000682276.1:n.1692G>A
ENST00000682892.1:c.1794G>A	ENSP00000507214.1:p.Glu598=
ENST00000682952.1:n.1886G>A
ENST00000684455.1:c.1460G>A
ENST00000684642.1:c.1644G>A	ENSP00000507355.1:p.Glu548=
ENST00000684740.1:n.2425G>A
ENST00000303236.9:c.2247G>A MANE Select	ENSP00000307235.3:p.Glu749=
ENST00000652099.1:c.2441G>A
ENST00000652736.1:n.2123G>A
ENST00000303236.7:c.2247G>A	ENSP00000307235.3:p.Glu749=
ENST00000415570.1:c.1884G>A	ENSP00000412076.1:p.Glu628=
ENST00000419748.5:c.1794G>A	ENSP00000408325.1:p.Glu598=
ENST00000470706.1:n.48+125G>A
NM_001313915.1:c.1794G>A	NP_001300844.1:p.Glu598=
NM_004836.5:c.2247G>A	NP_004827.4:p.Glu749=
NM_004836.6:c.2247G>A	NP_004827.4:p.Glu749=
NR_110236.1:n.1373C>T
XM_005264649.3:c.1563G>A	XP_005264706.1:p.Glu521=
XM_017005376.2:c.1563G>A	XP_016860865.1:p.Glu521=
NM_004836.7:c.2247G>A MANE Select	NP_004827.4:p.Glu749=
NM_001313915.2:c.1794G>A	NP_001300844.1:p.Glu598=