Canonical Allele Identifier: CA427445159

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874649G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575131G>T , CM000664.2:g.88575131G>T	GRCh38
NC_000002.11:g.88874649G>T , CM000664.1:g.88874649G>T	GRCh37
NC_000002.10:g.88655764G>T	NCBI36
NG_016424.1:g.57446C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2180C>A
ENST00000682276.1:n.1797C>A
ENST00000682892.1:c.1899C>A	ENSP00000507214.1:p.Ser633=
ENST00000682952.1:n.1991C>A
ENST00000684455.1:c.1565C>A
ENST00000684642.1:c.1749C>A	ENSP00000507355.1:p.Ser583=
ENST00000684740.1:n.2530C>A
ENST00000303236.9:c.2352C>A MANE Select	ENSP00000307235.3:p.Ser784=
ENST00000652099.1:c.2546C>A
ENST00000652736.1:n.2228C>A
ENST00000303236.7:c.2352C>A	ENSP00000307235.3:p.Ser784=
ENST00000415570.1:c.1989C>A	ENSP00000412076.1:p.Ser663=
ENST00000419748.5:c.1899C>A	ENSP00000408325.1:p.Ser633=
ENST00000470706.1:n.49-54C>A
NM_001313915.1:c.1899C>A	NP_001300844.1:p.Ser633=
NM_004836.5:c.2352C>A	NP_004827.4:p.Ser784=
NM_004836.6:c.2352C>A	NP_004827.4:p.Ser784=
NR_110236.1:n.1268G>T
XM_005264649.3:c.1668C>A	XP_005264706.1:p.Ser556=
XM_017005376.2:c.1668C>A	XP_016860865.1:p.Ser556=
NM_004836.7:c.2352C>A MANE Select	NP_004827.4:p.Ser784=
NM_001313915.2:c.1899C>A	NP_001300844.1:p.Ser633=