Canonical Allele Identifier: CA347592323

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874765T>C (hg19) ; chr2:g.88575247T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575247T>C , CM000664.2:g.88575247T>C	GRCh38
NC_000002.11:g.88874765T>C , CM000664.1:g.88874765T>C	GRCh37
NC_000002.10:g.88655880T>C	NCBI36
NG_016424.1:g.57330A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2064A>G
ENST00000682276.1:n.1681A>G
ENST00000682892.1:c.1783A>G	ENSP00000507214.1:p.Met595Val
ENST00000682952.1:n.1875A>G
ENST00000684455.1:c.1449A>G
ENST00000684642.1:c.1633A>G	ENSP00000507355.1:p.Met545Val
ENST00000684740.1:n.2414A>G
ENST00000303236.9:c.2236A>G MANE Select	ENSP00000307235.3:p.Met746Val
ENST00000652099.1:c.2430A>G
ENST00000652736.1:n.2112A>G
ENST00000303236.7:c.2236A>G	ENSP00000307235.3:p.Met746Val
ENST00000415570.1:c.1873A>G	ENSP00000412076.1:p.Met625Val
ENST00000419748.5:c.1783A>G	ENSP00000408325.1:p.Met595Val
ENST00000470706.1:n.48+114A>G
NM_001313915.1:c.1783A>G	NP_001300844.1:p.Met595Val
NM_004836.5:c.2236A>G	NP_004827.4:p.Met746Val
NM_004836.6:c.2236A>G	NP_004827.4:p.Met746Val
NR_110236.1:n.1384T>C
XM_005264649.3:c.1552A>G	XP_005264706.1:p.Met518Val
XM_017005376.2:c.1552A>G	XP_016860865.1:p.Met518Val
NM_004836.7:c.2236A>G MANE Select	NP_004827.4:p.Met746Val
NM_001313915.2:c.1783A>G	NP_001300844.1:p.Met595Val