Canonical Allele Identifier: CA2658632598
Gene: EIF2AK2 HGNC NCBI

Linked Data

gnomAD v4: 2-37149357-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.37149357T>G , CM000664.2:g.37149357T>G GRCh38
NC_000002.11:g.37376500T>G , CM000664.1:g.37376500T>G GRCh37
NC_000002.10:g.37230004T>G NCBI36
NG_030351.1:g.12691A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000233057.9:c.-183-334A>C MANE Select ENSP00000233057.4:n.-183-334A>C
ENST00000411537.7:n.29-334A>C
ENST00000679507.1:c.-16-1535A>C ENSP00000506024.1:n.-16-1535A>C
ENST00000679979.1:c.-183-334A>C ENSP00000506455.1:n.-183-334A>C
ENST00000680273.1:c.-183-334A>C ENSP00000506203.1:n.-183-334A>C
ENST00000681329.1:n.157-334A>C
ENST00000681463.1:c.-75-442A>C ENSP00000505138.1:n.-75-442A>C
ENST00000681507.1:c.-99-418A>C ENSP00000505772.1:n.-99-418A>C
ENST00000233057.8:c.-183-334A>C ENSP00000233057.4:n.-183-334A>C
ENST00000390013.3:c.-99-418A>C ENSP00000374663.3:n.-99-418A>C
ENST00000395127.6:c.-417-100A>C ENSP00000378559.2:n.-417-100A>C
ENST00000411537.6:c.-75-442A>C ENSP00000393921.2:n.-75-442A>C
NM_001135651.2:c.-183-334A>C NP_001129123.1:n.-183-334A>C
NM_002759.3:c.-417-100A>C NP_002750.1:n.-417-100A>C
XM_011532987.1:c.-99-418A>C XP_011531289.1:n.-99-418A>C
XM_011532987.2:c.-99-418A>C XP_011531289.1:n.-99-418A>C
XM_017004503.1:c.-183-334A>C XP_016859992.1:n.-183-334A>C
NM_001135651.3:c.-183-334A>C MANE Select NP_001129123.1:n.-183-334A>C
NM_002759.4:c.-417-100A>C NP_002750.1:n.-417-100A>C