Canonical Allele Identifier: CA347591485

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874582C>T (hg19) ; chr2:g.88575064C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575064C>T , CM000664.2:g.88575064C>T	GRCh38
NC_000002.11:g.88874582C>T , CM000664.1:g.88874582C>T	GRCh37
NC_000002.10:g.88655697C>T	NCBI36
NG_016424.1:g.57513G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2247G>A
ENST00000682276.1:n.1864G>A
ENST00000682892.1:c.1966G>A	ENSP00000507214.1:p.Val656Ile
ENST00000682952.1:n.2058G>A
ENST00000684455.1:c.1632G>A
ENST00000684642.1:c.1816G>A	ENSP00000507355.1:p.Val606Ile
ENST00000684740.1:n.2597G>A
ENST00000303236.9:c.2419G>A MANE Select	ENSP00000307235.3:p.Val807Ile
ENST00000652099.1:c.2613G>A
ENST00000652736.1:n.2295G>A
ENST00000303236.7:c.2419G>A	ENSP00000307235.3:p.Val807Ile
ENST00000415570.1:c.2056G>A	ENSP00000412076.1:p.Val686Ile
ENST00000419748.5:c.1966G>A	ENSP00000408325.1:p.Val656Ile
ENST00000470706.1:n.62G>A
NM_001313915.1:c.1966G>A	NP_001300844.1:p.Val656Ile
NM_004836.5:c.2419G>A	NP_004827.4:p.Val807Ile
NM_004836.6:c.2419G>A	NP_004827.4:p.Val807Ile
NR_110236.1:n.1201C>T
XM_005264649.3:c.1735G>A	XP_005264706.1:p.Val579Ile
XM_017005376.2:c.1735G>A	XP_016860865.1:p.Val579Ile
NM_004836.7:c.2419G>A MANE Select	NP_004827.4:p.Val807Ile
NM_001313915.2:c.1966G>A	NP_001300844.1:p.Val656Ile