Canonical Allele Identifier: CA347591422

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874570A>T (hg19) ; chr2:g.88575052A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575052A>T , CM000664.2:g.88575052A>T	GRCh38
NC_000002.11:g.88874570A>T , CM000664.1:g.88874570A>T	GRCh37
NC_000002.10:g.88655685A>T	NCBI36
NG_016424.1:g.57525T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2259T>A
ENST00000682276.1:n.1876T>A
ENST00000682892.1:c.1978T>A	ENSP00000507214.1:p.Ser660Thr
ENST00000682952.1:n.2070T>A
ENST00000684455.1:c.1644T>A
ENST00000684642.1:c.1828T>A	ENSP00000507355.1:p.Ser610Thr
ENST00000684740.1:n.2609T>A
ENST00000303236.9:c.2431T>A MANE Select	ENSP00000307235.3:p.Ser811Thr
ENST00000652099.1:c.2625T>A
ENST00000652736.1:n.2307T>A
ENST00000303236.7:c.2431T>A	ENSP00000307235.3:p.Ser811Thr
ENST00000415570.1:c.2068T>A	ENSP00000412076.1:p.Ser690Thr
ENST00000419748.5:c.1978T>A	ENSP00000408325.1:p.Ser660Thr
ENST00000470706.1:n.74T>A
NM_001313915.1:c.1978T>A	NP_001300844.1:p.Ser660Thr
NM_004836.5:c.2431T>A	NP_004827.4:p.Ser811Thr
NM_004836.6:c.2431T>A	NP_004827.4:p.Ser811Thr
NR_110236.1:n.1189A>T
XM_005264649.3:c.1747T>A	XP_005264706.1:p.Ser583Thr
XM_017005376.2:c.1747T>A	XP_016860865.1:p.Ser583Thr
NM_004836.7:c.2431T>A MANE Select	NP_004827.4:p.Ser811Thr
NM_001313915.2:c.1978T>A	NP_001300844.1:p.Ser660Thr