Canonical Allele Identifier: CA347592981
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575414A>T , CM000664.2:g.88575414A>T GRCh38
NC_000002.11:g.88874932A>T , CM000664.1:g.88874932A>T GRCh37
NC_000002.10:g.88656047A>T NCBI36
NG_016424.1:g.57163T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.1897T>A
ENST00000682276.1:n.1514T>A
ENST00000682892.1:c.1616T>A ENSP00000507214.1:p.Met539Lys
ENST00000682952.1:n.1708T>A
ENST00000684455.1:c.1282T>A
ENST00000684642.1:c.1466T>A ENSP00000507355.1:p.Met489Lys
ENST00000684740.1:n.2247T>A
ENST00000303236.9:c.2069T>A MANE Select ENSP00000307235.3:p.Met690Lys
ENST00000652099.1:c.2263T>A
ENST00000652736.1:n.1945T>A
ENST00000303236.7:c.2069T>A ENSP00000307235.3:p.Met690Lys
ENST00000415570.1:c.1706T>A ENSP00000412076.1:p.Met569Lys
ENST00000419748.5:c.1616T>A ENSP00000408325.1:p.Met539Lys
ENST00000478003.1:n.635T>A
NM_001313915.1:c.1616T>A NP_001300844.1:p.Met539Lys
NM_004836.5:c.2069T>A NP_004827.4:p.Met690Lys
NM_004836.6:c.2069T>A NP_004827.4:p.Met690Lys
NR_110236.1:n.1551A>T
XM_005264649.3:c.1385T>A XP_005264706.1:p.Met462Lys
XR_939749.1:n.2348T>A
XM_017005376.2:c.1385T>A XP_016860865.1:p.Met462Lys
NM_004836.7:c.2069T>A MANE Select NP_004827.4:p.Met690Lys
NM_001313915.2:c.1616T>A NP_001300844.1:p.Met539Lys