Canonical Allele Identifier: CA2660014814
Gene: EIF2AK3 HGNC NCBI

Linked Data

gnomAD v4: 2-88625014-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88625014G>T , CM000664.2:g.88625014G>T GRCh38
NC_000002.11:g.88924532G>T , CM000664.1:g.88924532G>T GRCh37
NC_000002.10:g.88705647G>T NCBI36
NG_016424.1:g.7563C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682892.1:c.-145-11161C>A ENSP00000507214.1:n.-145-11161C>A
ENST00000303236.9:c.308+1953C>A MANE Select ENSP00000307235.3:n.308+1953C>A
ENST00000652099.1:c.306+1953C>A
ENST00000652423.1:c.184+1953C>A ENSP00000498948.1:n.184+1953C>A
ENST00000303236.7:c.308+1953C>A ENSP00000307235.3:n.308+1953C>A
NM_004836.5:c.308+1953C>A NP_004827.4:n.308+1953C>A
NM_004836.6:c.308+1953C>A NP_004827.4:n.308+1953C>A
XR_939749.1:n.517+1953C>A
XM_017005376.2:c.-573+1953C>A XP_016860865.1:n.-573+1953C>A
NM_004836.7:c.308+1953C>A MANE Select NP_004827.4:n.308+1953C>A