Canonical Allele Identifier: CA347592937

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874912T>A (hg19) ; chr2:g.88575394T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575394T>A , CM000664.2:g.88575394T>A	GRCh38
NC_000002.11:g.88874912T>A , CM000664.1:g.88874912T>A	GRCh37
NC_000002.10:g.88656027T>A	NCBI36
NG_016424.1:g.57183A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1917A>T
ENST00000682276.1:n.1534A>T
ENST00000682892.1:c.1636A>T	ENSP00000507214.1:p.Ile546Leu
ENST00000682952.1:n.1728A>T
ENST00000684455.1:c.1302A>T
ENST00000684642.1:c.1486A>T	ENSP00000507355.1:p.Ile496Leu
ENST00000684740.1:n.2267A>T
ENST00000303236.9:c.2089A>T MANE Select	ENSP00000307235.3:p.Ile697Leu
ENST00000652099.1:c.2283A>T
ENST00000652736.1:n.1965A>T
ENST00000303236.7:c.2089A>T	ENSP00000307235.3:p.Ile697Leu
ENST00000415570.1:c.1726A>T	ENSP00000412076.1:p.Ile576Leu
ENST00000419748.5:c.1636A>T	ENSP00000408325.1:p.Ile546Leu
ENST00000470706.1:n.15A>T
ENST00000478003.1:n.655A>T
NM_001313915.1:c.1636A>T	NP_001300844.1:p.Ile546Leu
NM_004836.5:c.2089A>T	NP_004827.4:p.Ile697Leu
NM_004836.6:c.2089A>T	NP_004827.4:p.Ile697Leu
NR_110236.1:n.1531T>A
XM_005264649.3:c.1405A>T	XP_005264706.1:p.Ile469Leu
XR_939749.1:n.2368A>T
XM_017005376.2:c.1405A>T	XP_016860865.1:p.Ile469Leu
NM_004836.7:c.2089A>T MANE Select	NP_004827.4:p.Ile697Leu
NM_001313915.2:c.1636A>T	NP_001300844.1:p.Ile546Leu