Canonical Allele Identifier: CA347591776

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874648A>C (hg19) ; chr2:g.88575130A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575130A>C , CM000664.2:g.88575130A>C	GRCh38
NC_000002.11:g.88874648A>C , CM000664.1:g.88874648A>C	GRCh37
NC_000002.10:g.88655763A>C	NCBI36
NG_016424.1:g.57447T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2181T>G
ENST00000682276.1:n.1798T>G
ENST00000682892.1:c.1900T>G	ENSP00000507214.1:p.Phe634Val
ENST00000682952.1:n.1992T>G
ENST00000684455.1:c.1566T>G
ENST00000684642.1:c.1750T>G	ENSP00000507355.1:p.Phe584Val
ENST00000684740.1:n.2531T>G
ENST00000303236.9:c.2353T>G MANE Select	ENSP00000307235.3:p.Phe785Val
ENST00000652099.1:c.2547T>G
ENST00000652736.1:n.2229T>G
ENST00000303236.7:c.2353T>G	ENSP00000307235.3:p.Phe785Val
ENST00000415570.1:c.1990T>G	ENSP00000412076.1:p.Phe664Val
ENST00000419748.5:c.1900T>G	ENSP00000408325.1:p.Phe634Val
ENST00000470706.1:n.49-53T>G
NM_001313915.1:c.1900T>G	NP_001300844.1:p.Phe634Val
NM_004836.5:c.2353T>G	NP_004827.4:p.Phe785Val
NM_004836.6:c.2353T>G	NP_004827.4:p.Phe785Val
NR_110236.1:n.1267A>C
XM_005264649.3:c.1669T>G	XP_005264706.1:p.Phe557Val
XM_017005376.2:c.1669T>G	XP_016860865.1:p.Phe557Val
NM_004836.7:c.2353T>G MANE Select	NP_004827.4:p.Phe785Val
NM_001313915.2:c.1900T>G	NP_001300844.1:p.Phe634Val