Canonical Allele Identifier: CA347592192

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874742C>G (hg19) ; chr2:g.88575224C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575224C>G , CM000664.2:g.88575224C>G	GRCh38
NC_000002.11:g.88874742C>G , CM000664.1:g.88874742C>G	GRCh37
NC_000002.10:g.88655857C>G	NCBI36
NG_016424.1:g.57353G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2087G>C
ENST00000682276.1:n.1704G>C
ENST00000682892.1:c.1806G>C	ENSP00000507214.1:p.Glu602Asp
ENST00000682952.1:n.1898G>C
ENST00000684455.1:c.1472G>C
ENST00000684642.1:c.1656G>C	ENSP00000507355.1:p.Glu552Asp
ENST00000684740.1:n.2437G>C
ENST00000303236.9:c.2259G>C MANE Select	ENSP00000307235.3:p.Glu753Asp
ENST00000652099.1:c.2453G>C
ENST00000652736.1:n.2135G>C
ENST00000303236.7:c.2259G>C	ENSP00000307235.3:p.Glu753Asp
ENST00000415570.1:c.1896G>C	ENSP00000412076.1:p.Glu632Asp
ENST00000419748.5:c.1806G>C	ENSP00000408325.1:p.Glu602Asp
ENST00000470706.1:n.48+137G>C
NM_001313915.1:c.1806G>C	NP_001300844.1:p.Glu602Asp
NM_004836.5:c.2259G>C	NP_004827.4:p.Glu753Asp
NM_004836.6:c.2259G>C	NP_004827.4:p.Glu753Asp
NR_110236.1:n.1361C>G
XM_005264649.3:c.1575G>C	XP_005264706.1:p.Glu525Asp
XM_017005376.2:c.1575G>C	XP_016860865.1:p.Glu525Asp
NM_004836.7:c.2259G>C MANE Select	NP_004827.4:p.Glu753Asp
NM_001313915.2:c.1806G>C	NP_001300844.1:p.Glu602Asp