Canonical Allele Identifier: CA347592918
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575383C>A , CM000664.2:g.88575383C>A GRCh38
NC_000002.11:g.88874901C>A , CM000664.1:g.88874901C>A GRCh37
NC_000002.10:g.88656016C>A NCBI36
NG_016424.1:g.57194G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.1928G>T
ENST00000682276.1:n.1545G>T
ENST00000682892.1:c.1647G>T ENSP00000507214.1:p.Met549Ile
ENST00000682952.1:n.1739G>T
ENST00000684455.1:c.1313G>T
ENST00000684642.1:c.1497G>T ENSP00000507355.1:p.Met499Ile
ENST00000684740.1:n.2278G>T
ENST00000303236.9:c.2100G>T MANE Select ENSP00000307235.3:p.Met700Ile
ENST00000652099.1:c.2294G>T
ENST00000652736.1:n.1976G>T
ENST00000303236.7:c.2100G>T ENSP00000307235.3:p.Met700Ile
ENST00000415570.1:c.1737G>T ENSP00000412076.1:p.Met579Ile
ENST00000419748.5:c.1647G>T ENSP00000408325.1:p.Met549Ile
ENST00000470706.1:n.26G>T
ENST00000478003.1:n.666G>T
NM_001313915.1:c.1647G>T NP_001300844.1:p.Met549Ile
NM_004836.5:c.2100G>T NP_004827.4:p.Met700Ile
NM_004836.6:c.2100G>T NP_004827.4:p.Met700Ile
NR_110236.1:n.1520C>A
XM_005264649.3:c.1416G>T XP_005264706.1:p.Met472Ile
XR_939749.1:n.2379G>T
XM_017005376.2:c.1416G>T XP_016860865.1:p.Met472Ile
NM_004836.7:c.2100G>T MANE Select NP_004827.4:p.Met700Ile
NM_001313915.2:c.1647G>T NP_001300844.1:p.Met549Ile