Canonical Allele Identifier: CA427445568

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874592G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575074G>T , CM000664.2:g.88575074G>T	GRCh38
NC_000002.11:g.88874592G>T , CM000664.1:g.88874592G>T	GRCh37
NC_000002.10:g.88655707G>T	NCBI36
NG_016424.1:g.57503C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2237C>A
ENST00000682276.1:n.1854C>A
ENST00000682892.1:c.1956C>A	ENSP00000507214.1:p.Ser652=
ENST00000682952.1:n.2048C>A
ENST00000684455.1:c.1622C>A
ENST00000684642.1:c.1806C>A	ENSP00000507355.1:p.Ser602=
ENST00000684740.1:n.2587C>A
ENST00000303236.9:c.2409C>A MANE Select	ENSP00000307235.3:p.Ser803=
ENST00000652099.1:c.2603C>A
ENST00000652736.1:n.2285C>A
ENST00000303236.7:c.2409C>A	ENSP00000307235.3:p.Ser803=
ENST00000415570.1:c.2046C>A	ENSP00000412076.1:p.Ser682=
ENST00000419748.5:c.1956C>A	ENSP00000408325.1:p.Ser652=
ENST00000470706.1:n.52C>A
NM_001313915.1:c.1956C>A	NP_001300844.1:p.Ser652=
NM_004836.5:c.2409C>A	NP_004827.4:p.Ser803=
NM_004836.6:c.2409C>A	NP_004827.4:p.Ser803=
NR_110236.1:n.1211G>T
XM_005264649.3:c.1725C>A	XP_005264706.1:p.Ser575=
XM_017005376.2:c.1725C>A	XP_016860865.1:p.Ser575=
NM_004836.7:c.2409C>A MANE Select	NP_004827.4:p.Ser803=
NM_001313915.2:c.1956C>A	NP_001300844.1:p.Ser652=