Canonical Allele Identifier: CA347591588

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874606T>A (hg19) ; chr2:g.88575088T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575088T>A , CM000664.2:g.88575088T>A	GRCh38
NC_000002.11:g.88874606T>A , CM000664.1:g.88874606T>A	GRCh37
NC_000002.10:g.88655721T>A	NCBI36
NG_016424.1:g.57489A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2223A>T
ENST00000682276.1:n.1840A>T
ENST00000682892.1:c.1942A>T	ENSP00000507214.1:p.Arg648Trp
ENST00000682952.1:n.2034A>T
ENST00000684455.1:c.1608A>T
ENST00000684642.1:c.1792A>T	ENSP00000507355.1:p.Arg598Trp
ENST00000684740.1:n.2573A>T
ENST00000303236.9:c.2395A>T MANE Select	ENSP00000307235.3:p.Arg799Trp
ENST00000652099.1:c.2589A>T
ENST00000652736.1:n.2271A>T
ENST00000303236.7:c.2395A>T	ENSP00000307235.3:p.Arg799Trp
ENST00000415570.1:c.2032A>T	ENSP00000412076.1:p.Arg678Trp
ENST00000419748.5:c.1942A>T	ENSP00000408325.1:p.Arg648Trp
ENST00000470706.1:n.49-11A>T
NM_001313915.1:c.1942A>T	NP_001300844.1:p.Arg648Trp
NM_004836.5:c.2395A>T	NP_004827.4:p.Arg799Trp
NM_004836.6:c.2395A>T	NP_004827.4:p.Arg799Trp
NR_110236.1:n.1225T>A
XM_005264649.3:c.1711A>T	XP_005264706.1:p.Arg571Trp
XM_017005376.2:c.1711A>T	XP_016860865.1:p.Arg571Trp
NM_004836.7:c.2395A>T MANE Select	NP_004827.4:p.Arg799Trp
NM_001313915.2:c.1942A>T	NP_001300844.1:p.Arg648Trp