Canonical Allele Identifier: CA347592155

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874734T>A (hg19) ; chr2:g.88575216T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575216T>A , CM000664.2:g.88575216T>A	GRCh38
NC_000002.11:g.88874734T>A , CM000664.1:g.88874734T>A	GRCh37
NC_000002.10:g.88655849T>A	NCBI36
NG_016424.1:g.57361A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2095A>T
ENST00000682276.1:n.1712A>T
ENST00000682892.1:c.1814A>T	ENSP00000507214.1:p.Asp605Val
ENST00000682952.1:n.1906A>T
ENST00000684455.1:c.1480A>T
ENST00000684642.1:c.1664A>T	ENSP00000507355.1:p.Asp555Val
ENST00000684740.1:n.2445A>T
ENST00000303236.9:c.2267A>T MANE Select	ENSP00000307235.3:p.Asp756Val
ENST00000652099.1:c.2461A>T
ENST00000652736.1:n.2143A>T
ENST00000303236.7:c.2267A>T	ENSP00000307235.3:p.Asp756Val
ENST00000415570.1:c.1904A>T	ENSP00000412076.1:p.Asp635Val
ENST00000419748.5:c.1814A>T	ENSP00000408325.1:p.Asp605Val
ENST00000470706.1:n.49-139A>T
NM_001313915.1:c.1814A>T	NP_001300844.1:p.Asp605Val
NM_004836.5:c.2267A>T	NP_004827.4:p.Asp756Val
NM_004836.6:c.2267A>T	NP_004827.4:p.Asp756Val
NR_110236.1:n.1353T>A
XM_005264649.3:c.1583A>T	XP_005264706.1:p.Asp528Val
XM_017005376.2:c.1583A>T	XP_016860865.1:p.Asp528Val
NM_004836.7:c.2267A>T MANE Select	NP_004827.4:p.Asp756Val
NM_001313915.2:c.1814A>T	NP_001300844.1:p.Asp605Val