Canonical Allele Identifier: CA347591585

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874605C>G (hg19) ; chr2:g.88575087C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575087C>G , CM000664.2:g.88575087C>G	GRCh38
NC_000002.11:g.88874605C>G , CM000664.1:g.88874605C>G	GRCh37
NC_000002.10:g.88655720C>G	NCBI36
NG_016424.1:g.57490G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2224G>C
ENST00000682276.1:n.1841G>C
ENST00000682892.1:c.1943G>C	ENSP00000507214.1:p.Arg648Thr
ENST00000682952.1:n.2035G>C
ENST00000684455.1:c.1609G>C
ENST00000684642.1:c.1793G>C	ENSP00000507355.1:p.Arg598Thr
ENST00000684740.1:n.2574G>C
ENST00000303236.9:c.2396G>C MANE Select	ENSP00000307235.3:p.Arg799Thr
ENST00000652099.1:c.2590G>C
ENST00000652736.1:n.2272G>C
ENST00000303236.7:c.2396G>C	ENSP00000307235.3:p.Arg799Thr
ENST00000415570.1:c.2033G>C	ENSP00000412076.1:p.Arg678Thr
ENST00000419748.5:c.1943G>C	ENSP00000408325.1:p.Arg648Thr
ENST00000470706.1:n.49-10G>C
NM_001313915.1:c.1943G>C	NP_001300844.1:p.Arg648Thr
NM_004836.5:c.2396G>C	NP_004827.4:p.Arg799Thr
NM_004836.6:c.2396G>C	NP_004827.4:p.Arg799Thr
NR_110236.1:n.1224C>G
XM_005264649.3:c.1712G>C	XP_005264706.1:p.Arg571Thr
XM_017005376.2:c.1712G>C	XP_016860865.1:p.Arg571Thr
NM_004836.7:c.2396G>C MANE Select	NP_004827.4:p.Arg799Thr
NM_001313915.2:c.1943G>C	NP_001300844.1:p.Arg648Thr