Canonical Allele Identifier: CA347592435

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874792G>T (hg19) ; chr2:g.88575274G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575274G>T , CM000664.2:g.88575274G>T	GRCh38
NC_000002.11:g.88874792G>T , CM000664.1:g.88874792G>T	GRCh37
NC_000002.10:g.88655907G>T	NCBI36
NG_016424.1:g.57303C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000478003.2:n.2037C>A
ENST00000682276.1:n.1654C>A
ENST00000682892.1:c.1756C>A	ENSP00000507214.1:p.Gln586Lys
ENST00000682952.1:n.1848C>A
ENST00000684455.1:c.1422C>A
ENST00000684642.1:c.1606C>A	ENSP00000507355.1:p.Gln536Lys
ENST00000684740.1:n.2387C>A
ENST00000303236.9:c.2209C>A MANE Select	ENSP00000307235.3:p.Gln737Lys
ENST00000652099.1:c.2403C>A
ENST00000652736.1:n.2085C>A
ENST00000303236.7:c.2209C>A	ENSP00000307235.3:p.Gln737Lys
ENST00000415570.1:c.1846C>A	ENSP00000412076.1:p.Gln616Lys
ENST00000419748.5:c.1756C>A	ENSP00000408325.1:p.Gln586Lys
ENST00000470706.1:n.48+87C>A
NM_001313915.1:c.1756C>A	NP_001300844.1:p.Gln586Lys
NM_004836.5:c.2209C>A	NP_004827.4:p.Gln737Lys
NM_004836.6:c.2209C>A	NP_004827.4:p.Gln737Lys
NR_110236.1:n.1411G>T
XM_005264649.3:c.1525C>A	XP_005264706.1:p.Gln509Lys
XR_939749.1:n.2488C>A
XM_017005376.2:c.1525C>A	XP_016860865.1:p.Gln509Lys
NM_004836.7:c.2209C>A MANE Select	NP_004827.4:p.Gln737Lys
NM_001313915.2:c.1756C>A	NP_001300844.1:p.Gln586Lys