Canonical Allele Identifier: CA427445302

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874712G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575194G>A , CM000664.2:g.88575194G>A	GRCh38
NC_000002.11:g.88874712G>A , CM000664.1:g.88874712G>A	GRCh37
NC_000002.10:g.88655827G>A	NCBI36
NG_016424.1:g.57383C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000478003.2:n.2117C>T
ENST00000682276.1:n.1734C>T
ENST00000682892.1:c.1836C>T	ENSP00000507214.1:p.Asp612=
ENST00000682952.1:n.1928C>T
ENST00000684455.1:c.1502C>T
ENST00000684642.1:c.1686C>T	ENSP00000507355.1:p.Asp562=
ENST00000684740.1:n.2467C>T
ENST00000303236.9:c.2289C>T MANE Select	ENSP00000307235.3:p.Asp763=
ENST00000652099.1:c.2483C>T
ENST00000652736.1:n.2165C>T
ENST00000303236.7:c.2289C>T	ENSP00000307235.3:p.Asp763=
ENST00000415570.1:c.1926C>T	ENSP00000412076.1:p.Asp642=
ENST00000419748.5:c.1836C>T	ENSP00000408325.1:p.Asp612=
ENST00000470706.1:n.49-117C>T
NM_001313915.1:c.1836C>T	NP_001300844.1:p.Asp612=
NM_004836.5:c.2289C>T	NP_004827.4:p.Asp763=
NM_004836.6:c.2289C>T	NP_004827.4:p.Asp763=
NR_110236.1:n.1331G>A
XM_005264649.3:c.1605C>T	XP_005264706.1:p.Asp535=
XM_017005376.2:c.1605C>T	XP_016860865.1:p.Asp535=
NM_004836.7:c.2289C>T MANE Select	NP_004827.4:p.Asp763=
NM_001313915.2:c.1836C>T	NP_001300844.1:p.Asp612=