Canonical Allele Identifier: CA347591526

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874591A>T (hg19) ; chr2:g.88575073A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575073A>T , CM000664.2:g.88575073A>T	GRCh38
NC_000002.11:g.88874591A>T , CM000664.1:g.88874591A>T	GRCh37
NC_000002.10:g.88655706A>T	NCBI36
NG_016424.1:g.57504T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2238T>A
ENST00000682276.1:n.1855T>A
ENST00000682892.1:c.1957T>A	ENSP00000507214.1:p.Ser653Thr
ENST00000682952.1:n.2049T>A
ENST00000684455.1:c.1623T>A
ENST00000684642.1:c.1807T>A	ENSP00000507355.1:p.Ser603Thr
ENST00000684740.1:n.2588T>A
ENST00000303236.9:c.2410T>A MANE Select	ENSP00000307235.3:p.Ser804Thr
ENST00000652099.1:c.2604T>A
ENST00000652736.1:n.2286T>A
ENST00000303236.7:c.2410T>A	ENSP00000307235.3:p.Ser804Thr
ENST00000415570.1:c.2047T>A	ENSP00000412076.1:p.Ser683Thr
ENST00000419748.5:c.1957T>A	ENSP00000408325.1:p.Ser653Thr
ENST00000470706.1:n.53T>A
NM_001313915.1:c.1957T>A	NP_001300844.1:p.Ser653Thr
NM_004836.5:c.2410T>A	NP_004827.4:p.Ser804Thr
NM_004836.6:c.2410T>A	NP_004827.4:p.Ser804Thr
NR_110236.1:n.1210A>T
XM_005264649.3:c.1726T>A	XP_005264706.1:p.Ser576Thr
XM_017005376.2:c.1726T>A	XP_016860865.1:p.Ser576Thr
NM_004836.7:c.2410T>A MANE Select	NP_004827.4:p.Ser804Thr
NM_001313915.2:c.1957T>A	NP_001300844.1:p.Ser653Thr