Canonical Allele Identifier: CA347591967

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874695C>T (hg19) ; chr2:g.88575177C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575177C>T , CM000664.2:g.88575177C>T	GRCh38
NC_000002.11:g.88874695C>T , CM000664.1:g.88874695C>T	GRCh37
NC_000002.10:g.88655810C>T	NCBI36
NG_016424.1:g.57400G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2134G>A
ENST00000682276.1:n.1751G>A
ENST00000682892.1:c.1853G>A	ENSP00000507214.1:p.Cys618Tyr
ENST00000682952.1:n.1945G>A
ENST00000684455.1:c.1519G>A
ENST00000684642.1:c.1703G>A	ENSP00000507355.1:p.Cys568Tyr
ENST00000684740.1:n.2484G>A
ENST00000303236.9:c.2306G>A MANE Select	ENSP00000307235.3:p.Cys769Tyr
ENST00000652099.1:c.2500G>A
ENST00000652736.1:n.2182G>A
ENST00000303236.7:c.2306G>A	ENSP00000307235.3:p.Cys769Tyr
ENST00000415570.1:c.1943G>A	ENSP00000412076.1:p.Cys648Tyr
ENST00000419748.5:c.1853G>A	ENSP00000408325.1:p.Cys618Tyr
ENST00000470706.1:n.49-100G>A
NM_001313915.1:c.1853G>A	NP_001300844.1:p.Cys618Tyr
NM_004836.5:c.2306G>A	NP_004827.4:p.Cys769Tyr
NM_004836.6:c.2306G>A	NP_004827.4:p.Cys769Tyr
NR_110236.1:n.1314C>T
XM_005264649.3:c.1622G>A	XP_005264706.1:p.Cys541Tyr
XM_017005376.2:c.1622G>A	XP_016860865.1:p.Cys541Tyr
NM_004836.7:c.2306G>A MANE Select	NP_004827.4:p.Cys769Tyr
NM_001313915.2:c.1853G>A	NP_001300844.1:p.Cys618Tyr