Canonical Allele Identifier: CA427445220

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874679C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575161C>G , CM000664.2:g.88575161C>G	GRCh38
NC_000002.11:g.88874679C>G , CM000664.1:g.88874679C>G	GRCh37
NC_000002.10:g.88655794C>G	NCBI36
NG_016424.1:g.57416G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2150G>C
ENST00000682276.1:n.1767G>C
ENST00000682892.1:c.1869G>C	ENSP00000507214.1:p.Gly623=
ENST00000682952.1:n.1961G>C
ENST00000684455.1:c.1535G>C
ENST00000684642.1:c.1719G>C	ENSP00000507355.1:p.Gly573=
ENST00000684740.1:n.2500G>C
ENST00000303236.9:c.2322G>C MANE Select	ENSP00000307235.3:p.Gly774=
ENST00000652099.1:c.2516G>C
ENST00000652736.1:n.2198G>C
ENST00000303236.7:c.2322G>C	ENSP00000307235.3:p.Gly774=
ENST00000415570.1:c.1959G>C	ENSP00000412076.1:p.Gly653=
ENST00000419748.5:c.1869G>C	ENSP00000408325.1:p.Gly623=
ENST00000470706.1:n.49-84G>C
NM_001313915.1:c.1869G>C	NP_001300844.1:p.Gly623=
NM_004836.5:c.2322G>C	NP_004827.4:p.Gly774=
NM_004836.6:c.2322G>C	NP_004827.4:p.Gly774=
NR_110236.1:n.1298C>G
XM_005264649.3:c.1638G>C	XP_005264706.1:p.Gly546=
XM_017005376.2:c.1638G>C	XP_016860865.1:p.Gly546=
NM_004836.7:c.2322G>C MANE Select	NP_004827.4:p.Gly774=
NM_001313915.2:c.1869G>C	NP_001300844.1:p.Gly623=