Canonical Allele Identifier: CA347592138

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874731G>A (hg19) ; chr2:g.88575213G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575213G>A , CM000664.2:g.88575213G>A	GRCh38
NC_000002.11:g.88874731G>A , CM000664.1:g.88874731G>A	GRCh37
NC_000002.10:g.88655846G>A	NCBI36
NG_016424.1:g.57364C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2098C>T
ENST00000682276.1:n.1715C>T
ENST00000682892.1:c.1817C>T	ENSP00000507214.1:p.Ala606Val
ENST00000682952.1:n.1909C>T
ENST00000684455.1:c.1483C>T
ENST00000684642.1:c.1667C>T	ENSP00000507355.1:p.Ala556Val
ENST00000684740.1:n.2448C>T
ENST00000303236.9:c.2270C>T MANE Select	ENSP00000307235.3:p.Ala757Val
ENST00000652099.1:c.2464C>T
ENST00000652736.1:n.2146C>T
ENST00000303236.7:c.2270C>T	ENSP00000307235.3:p.Ala757Val
ENST00000415570.1:c.1907C>T	ENSP00000412076.1:p.Ala636Val
ENST00000419748.5:c.1817C>T	ENSP00000408325.1:p.Ala606Val
ENST00000470706.1:n.49-136C>T
NM_001313915.1:c.1817C>T	NP_001300844.1:p.Ala606Val
NM_004836.5:c.2270C>T	NP_004827.4:p.Ala757Val
NM_004836.6:c.2270C>T	NP_004827.4:p.Ala757Val
NR_110236.1:n.1350G>A
XM_005264649.3:c.1586C>T	XP_005264706.1:p.Ala529Val
XM_017005376.2:c.1586C>T	XP_016860865.1:p.Ala529Val
NM_004836.7:c.2270C>T MANE Select	NP_004827.4:p.Ala757Val
NM_001313915.2:c.1817C>T	NP_001300844.1:p.Ala606Val