Canonical Allele Identifier: CA347592032

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874709A>C (hg19) ; chr2:g.88575191A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575191A>C , CM000664.2:g.88575191A>C	GRCh38
NC_000002.11:g.88874709A>C , CM000664.1:g.88874709A>C	GRCh37
NC_000002.10:g.88655824A>C	NCBI36
NG_016424.1:g.57386T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000478003.2:n.2120T>G
ENST00000682276.1:n.1737T>G
ENST00000682892.1:c.1839T>G	ENSP00000507214.1:p.Ser613Arg
ENST00000682952.1:n.1931T>G
ENST00000684455.1:c.1505T>G
ENST00000684642.1:c.1689T>G	ENSP00000507355.1:p.Ser563Arg
ENST00000684740.1:n.2470T>G
ENST00000303236.9:c.2292T>G MANE Select	ENSP00000307235.3:p.Ser764Arg
ENST00000652099.1:c.2486T>G
ENST00000652736.1:n.2168T>G
ENST00000303236.7:c.2292T>G	ENSP00000307235.3:p.Ser764Arg
ENST00000415570.1:c.1929T>G	ENSP00000412076.1:p.Ser643Arg
ENST00000419748.5:c.1839T>G	ENSP00000408325.1:p.Ser613Arg
ENST00000470706.1:n.49-114T>G
NM_001313915.1:c.1839T>G	NP_001300844.1:p.Ser613Arg
NM_004836.5:c.2292T>G	NP_004827.4:p.Ser764Arg
NM_004836.6:c.2292T>G	NP_004827.4:p.Ser764Arg
NR_110236.1:n.1328A>C
XM_005264649.3:c.1608T>G	XP_005264706.1:p.Ser536Arg
XM_017005376.2:c.1608T>G	XP_016860865.1:p.Ser536Arg
NM_004836.7:c.2292T>G MANE Select	NP_004827.4:p.Ser764Arg
NM_001313915.2:c.1839T>G	NP_001300844.1:p.Ser613Arg