Canonical Allele Identifier: CA347592984
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575415T>G , CM000664.2:g.88575415T>G GRCh38
NC_000002.11:g.88874933T>G , CM000664.1:g.88874933T>G GRCh37
NC_000002.10:g.88656048T>G NCBI36
NG_016424.1:g.57162A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.1896A>C
ENST00000682276.1:n.1513A>C
ENST00000682892.1:c.1615A>C ENSP00000507214.1:p.Met539Leu
ENST00000682952.1:n.1707A>C
ENST00000684455.1:c.1281A>C
ENST00000684642.1:c.1465A>C ENSP00000507355.1:p.Met489Leu
ENST00000684740.1:n.2246A>C
ENST00000303236.9:c.2068A>C MANE Select ENSP00000307235.3:p.Met690Leu
ENST00000652099.1:c.2262A>C
ENST00000652736.1:n.1944A>C
ENST00000303236.7:c.2068A>C ENSP00000307235.3:p.Met690Leu
ENST00000415570.1:c.1705A>C ENSP00000412076.1:p.Met569Leu
ENST00000419748.5:c.1615A>C ENSP00000408325.1:p.Met539Leu
ENST00000478003.1:n.634A>C
NM_001313915.1:c.1615A>C NP_001300844.1:p.Met539Leu
NM_004836.5:c.2068A>C NP_004827.4:p.Met690Leu
NM_004836.6:c.2068A>C NP_004827.4:p.Met690Leu
NR_110236.1:n.1552T>G
XM_005264649.3:c.1384A>C XP_005264706.1:p.Met462Leu
XR_939749.1:n.2347A>C
XM_017005376.2:c.1384A>C XP_016860865.1:p.Met462Leu
NM_004836.7:c.2068A>C MANE Select NP_004827.4:p.Met690Leu
NM_001313915.2:c.1615A>C NP_001300844.1:p.Met539Leu