Canonical Allele Identifier: CA347592990

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874936G>T (hg19) ; chr2:g.88575418G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575418G>T , CM000664.2:g.88575418G>T	GRCh38
NC_000002.11:g.88874936G>T , CM000664.1:g.88874936G>T	GRCh37
NC_000002.10:g.88656051G>T	NCBI36
NG_016424.1:g.57159C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1893C>A
ENST00000682276.1:n.1510C>A
ENST00000682892.1:c.1612C>A	ENSP00000507214.1:p.Pro538Thr
ENST00000682952.1:n.1704C>A
ENST00000684455.1:c.1278C>A
ENST00000684642.1:c.1462C>A	ENSP00000507355.1:p.Pro488Thr
ENST00000684740.1:n.2243C>A
ENST00000303236.9:c.2065C>A MANE Select	ENSP00000307235.3:p.Pro689Thr
ENST00000652099.1:c.2259C>A
ENST00000652736.1:n.1941C>A
ENST00000303236.7:c.2065C>A	ENSP00000307235.3:p.Pro689Thr
ENST00000415570.1:c.1702C>A	ENSP00000412076.1:p.Pro568Thr
ENST00000419748.5:c.1612C>A	ENSP00000408325.1:p.Pro538Thr
ENST00000478003.1:n.631C>A
NM_001313915.1:c.1612C>A	NP_001300844.1:p.Pro538Thr
NM_004836.5:c.2065C>A	NP_004827.4:p.Pro689Thr
NM_004836.6:c.2065C>A	NP_004827.4:p.Pro689Thr
NR_110236.1:n.1555G>T
XM_005264649.3:c.1381C>A	XP_005264706.1:p.Pro461Thr
XR_939749.1:n.2344C>A
XM_017005376.2:c.1381C>A	XP_016860865.1:p.Pro461Thr
NM_004836.7:c.2065C>A MANE Select	NP_004827.4:p.Pro689Thr
NM_001313915.2:c.1612C>A	NP_001300844.1:p.Pro538Thr