Canonical Allele Identifier: CA347591575

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874603C>G (hg19) ; chr2:g.88575085C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575085C>G , CM000664.2:g.88575085C>G	GRCh38
NC_000002.11:g.88874603C>G , CM000664.1:g.88874603C>G	GRCh37
NC_000002.10:g.88655718C>G	NCBI36
NG_016424.1:g.57492G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2226G>C
ENST00000682276.1:n.1843G>C
ENST00000682892.1:c.1945G>C	ENSP00000507214.1:p.Glu649Gln
ENST00000682952.1:n.2037G>C
ENST00000684455.1:c.1611G>C
ENST00000684642.1:c.1795G>C	ENSP00000507355.1:p.Glu599Gln
ENST00000684740.1:n.2576G>C
ENST00000303236.9:c.2398G>C MANE Select	ENSP00000307235.3:p.Glu800Gln
ENST00000652099.1:c.2592G>C
ENST00000652736.1:n.2274G>C
ENST00000303236.7:c.2398G>C	ENSP00000307235.3:p.Glu800Gln
ENST00000415570.1:c.2035G>C	ENSP00000412076.1:p.Glu679Gln
ENST00000419748.5:c.1945G>C	ENSP00000408325.1:p.Glu649Gln
ENST00000470706.1:n.49-8G>C
NM_001313915.1:c.1945G>C	NP_001300844.1:p.Glu649Gln
NM_004836.5:c.2398G>C	NP_004827.4:p.Glu800Gln
NM_004836.6:c.2398G>C	NP_004827.4:p.Glu800Gln
NR_110236.1:n.1222C>G
XM_005264649.3:c.1714G>C	XP_005264706.1:p.Glu572Gln
XM_017005376.2:c.1714G>C	XP_016860865.1:p.Glu572Gln
NM_004836.7:c.2398G>C MANE Select	NP_004827.4:p.Glu800Gln
NM_001313915.2:c.1945G>C	NP_001300844.1:p.Glu649Gln