Canonical Allele Identifier: CA347592389

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874782G>T (hg19) ; chr2:g.88575264G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575264G>T , CM000664.2:g.88575264G>T	GRCh38
NC_000002.11:g.88874782G>T , CM000664.1:g.88874782G>T	GRCh37
NC_000002.10:g.88655897G>T	NCBI36
NG_016424.1:g.57313C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2047C>A
ENST00000682276.1:n.1664C>A
ENST00000682892.1:c.1766C>A	ENSP00000507214.1:p.Pro589Gln
ENST00000682952.1:n.1858C>A
ENST00000684455.1:c.1432C>A
ENST00000684642.1:c.1616C>A	ENSP00000507355.1:p.Pro539Gln
ENST00000684740.1:n.2397C>A
ENST00000303236.9:c.2219C>A MANE Select	ENSP00000307235.3:p.Pro740Gln
ENST00000652099.1:c.2413C>A
ENST00000652736.1:n.2095C>A
ENST00000303236.7:c.2219C>A	ENSP00000307235.3:p.Pro740Gln
ENST00000415570.1:c.1856C>A	ENSP00000412076.1:p.Pro619Gln
ENST00000419748.5:c.1766C>A	ENSP00000408325.1:p.Pro589Gln
ENST00000470706.1:n.48+97C>A
NM_001313915.1:c.1766C>A	NP_001300844.1:p.Pro589Gln
NM_004836.5:c.2219C>A	NP_004827.4:p.Pro740Gln
NM_004836.6:c.2219C>A	NP_004827.4:p.Pro740Gln
NR_110236.1:n.1401G>T
XM_005264649.3:c.1535C>A	XP_005264706.1:p.Pro512Gln
XR_939749.1:n.2498C>A
XM_017005376.2:c.1535C>A	XP_016860865.1:p.Pro512Gln
NM_004836.7:c.2219C>A MANE Select	NP_004827.4:p.Pro740Gln
NM_001313915.2:c.1766C>A	NP_001300844.1:p.Pro589Gln