Canonical Allele Identifier: CA347591611
Gene: EIF2AK3 HGNC NCBI

Linked Data

gnomAD v4: 2-88575093-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575093C>T , CM000664.2:g.88575093C>T GRCh38
NC_000002.11:g.88874611C>T , CM000664.1:g.88874611C>T GRCh37
NC_000002.10:g.88655726C>T NCBI36
NG_016424.1:g.57484G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2218G>A
ENST00000682276.1:n.1835G>A
ENST00000682892.1:c.1937G>A ENSP00000507214.1:p.Arg646Lys
ENST00000682952.1:n.2029G>A
ENST00000684455.1:c.1603G>A
ENST00000684642.1:c.1787G>A ENSP00000507355.1:p.Arg596Lys
ENST00000684740.1:n.2568G>A
ENST00000303236.9:c.2390G>A MANE Select ENSP00000307235.3:p.Arg797Lys
ENST00000652099.1:c.2584G>A
ENST00000652736.1:n.2266G>A
ENST00000303236.7:c.2390G>A ENSP00000307235.3:p.Arg797Lys
ENST00000415570.1:c.2027G>A ENSP00000412076.1:p.Arg676Lys
ENST00000419748.5:c.1937G>A ENSP00000408325.1:p.Arg646Lys
ENST00000470706.1:n.49-16G>A
NM_001313915.1:c.1937G>A NP_001300844.1:p.Arg646Lys
NM_004836.5:c.2390G>A NP_004827.4:p.Arg797Lys
NM_004836.6:c.2390G>A NP_004827.4:p.Arg797Lys
NR_110236.1:n.1230C>T
XM_005264649.3:c.1706G>A XP_005264706.1:p.Arg569Lys
XM_017005376.2:c.1706G>A XP_016860865.1:p.Arg569Lys
NM_004836.7:c.2390G>A MANE Select NP_004827.4:p.Arg797Lys
NM_001313915.2:c.1937G>A NP_001300844.1:p.Arg646Lys