Canonical Allele Identifier: CA2660014832
Gene: EIF2AK3 HGNC NCBI

Linked Data

gnomAD v4: 2-88625034-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88625034A>G , CM000664.2:g.88625034A>G GRCh38
NC_000002.11:g.88924552A>G , CM000664.1:g.88924552A>G GRCh37
NC_000002.10:g.88705667A>G NCBI36
NG_016424.1:g.7543T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682892.1:c.-145-11181T>C ENSP00000507214.1:n.-145-11181T>C
ENST00000303236.9:c.308+1933T>C MANE Select ENSP00000307235.3:n.308+1933T>C
ENST00000652099.1:c.306+1933T>C
ENST00000652423.1:c.184+1933T>C ENSP00000498948.1:n.184+1933T>C
ENST00000303236.7:c.308+1933T>C ENSP00000307235.3:n.308+1933T>C
NM_004836.5:c.308+1933T>C NP_004827.4:n.308+1933T>C
NM_004836.6:c.308+1933T>C NP_004827.4:n.308+1933T>C
XR_939749.1:n.517+1933T>C
XM_017005376.2:c.-573+1933T>C XP_016860865.1:n.-573+1933T>C
NM_004836.7:c.308+1933T>C MANE Select NP_004827.4:n.308+1933T>C