Canonical Allele Identifier: CA2658632641
Gene: EIF2AK2 HGNC NCBI

Linked Data

gnomAD v4: 2-37149415-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.37149415C>A , CM000664.2:g.37149415C>A GRCh38
NC_000002.11:g.37376558C>A , CM000664.1:g.37376558C>A GRCh37
NC_000002.10:g.37230062C>A NCBI36
NG_030351.1:g.12633G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233057.9:c.-183-392G>T MANE Select ENSP00000233057.4:n.-183-392G>T
ENST00000411537.7:n.29-392G>T
ENST00000679507.1:c.-16-1593G>T ENSP00000506024.1:n.-16-1593G>T
ENST00000679979.1:c.-183-392G>T ENSP00000506455.1:n.-183-392G>T
ENST00000680273.1:c.-183-392G>T ENSP00000506203.1:n.-183-392G>T
ENST00000681329.1:n.157-392G>T
ENST00000681463.1:c.-75-500G>T ENSP00000505138.1:n.-75-500G>T
ENST00000681507.1:c.-99-476G>T ENSP00000505772.1:n.-99-476G>T
ENST00000233057.8:c.-183-392G>T ENSP00000233057.4:n.-183-392G>T
ENST00000390013.3:c.-99-476G>T ENSP00000374663.3:n.-99-476G>T
ENST00000395127.6:c.-417-158G>T ENSP00000378559.2:n.-417-158G>T
ENST00000411537.6:c.-75-500G>T ENSP00000393921.2:n.-75-500G>T
NM_001135651.2:c.-183-392G>T NP_001129123.1:n.-183-392G>T
NM_002759.3:c.-417-158G>T NP_002750.1:n.-417-158G>T
XM_011532987.1:c.-99-476G>T XP_011531289.1:n.-99-476G>T
XM_011532987.2:c.-99-476G>T XP_011531289.1:n.-99-476G>T
XM_017004503.1:c.-183-392G>T XP_016859992.1:n.-183-392G>T
NM_001135651.3:c.-183-392G>T MANE Select NP_001129123.1:n.-183-392G>T
NM_002759.4:c.-417-158G>T NP_002750.1:n.-417-158G>T