Canonical Allele Identifier: CA427445534

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874580T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575062T>C , CM000664.2:g.88575062T>C	GRCh38
NC_000002.11:g.88874580T>C , CM000664.1:g.88874580T>C	GRCh37
NC_000002.10:g.88655695T>C	NCBI36
NG_016424.1:g.57515A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2249A>G
ENST00000682276.1:n.1866A>G
ENST00000682892.1:c.1968A>G	ENSP00000507214.1:p.Val656=
ENST00000682952.1:n.2060A>G
ENST00000684455.1:c.1634A>G
ENST00000684642.1:c.1818A>G	ENSP00000507355.1:p.Val606=
ENST00000684740.1:n.2599A>G
ENST00000303236.9:c.2421A>G MANE Select	ENSP00000307235.3:p.Val807=
ENST00000652099.1:c.2615A>G
ENST00000652736.1:n.2297A>G
ENST00000303236.7:c.2421A>G	ENSP00000307235.3:p.Val807=
ENST00000415570.1:c.2058A>G	ENSP00000412076.1:p.Val686=
ENST00000419748.5:c.1968A>G	ENSP00000408325.1:p.Val656=
ENST00000470706.1:n.64A>G
NM_001313915.1:c.1968A>G	NP_001300844.1:p.Val656=
NM_004836.5:c.2421A>G	NP_004827.4:p.Val807=
NM_004836.6:c.2421A>G	NP_004827.4:p.Val807=
NR_110236.1:n.1199T>C
XM_005264649.3:c.1737A>G	XP_005264706.1:p.Val579=
XM_017005376.2:c.1737A>G	XP_016860865.1:p.Val579=
NM_004836.7:c.2421A>G MANE Select	NP_004827.4:p.Val807=
NM_001313915.2:c.1968A>G	NP_001300844.1:p.Val656=