Canonical Allele Identifier: CA2658632652
Gene: EIF2AK2 HGNC NCBI

Linked Data

gnomAD v4: 2-37149428-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.37149428T>C , CM000664.2:g.37149428T>C GRCh38
NC_000002.11:g.37376571T>C , CM000664.1:g.37376571T>C GRCh37
NC_000002.10:g.37230075T>C NCBI36
NG_030351.1:g.12620A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000233057.9:c.-183-405A>G MANE Select ENSP00000233057.4:n.-183-405A>G
ENST00000411537.7:n.29-405A>G
ENST00000679507.1:c.-16-1606A>G ENSP00000506024.1:n.-16-1606A>G
ENST00000679979.1:c.-183-405A>G ENSP00000506455.1:n.-183-405A>G
ENST00000680273.1:c.-183-405A>G ENSP00000506203.1:n.-183-405A>G
ENST00000681329.1:n.157-405A>G
ENST00000681463.1:c.-75-513A>G ENSP00000505138.1:n.-75-513A>G
ENST00000681507.1:c.-99-489A>G ENSP00000505772.1:n.-99-489A>G
ENST00000233057.8:c.-183-405A>G ENSP00000233057.4:n.-183-405A>G
ENST00000390013.3:c.-99-489A>G ENSP00000374663.3:n.-99-489A>G
ENST00000395127.6:c.-417-171A>G ENSP00000378559.2:n.-417-171A>G
ENST00000411537.6:c.-75-513A>G ENSP00000393921.2:n.-75-513A>G
NM_001135651.2:c.-183-405A>G NP_001129123.1:n.-183-405A>G
NM_002759.3:c.-417-171A>G NP_002750.1:n.-417-171A>G
XM_011532987.1:c.-99-489A>G XP_011531289.1:n.-99-489A>G
XM_011532987.2:c.-99-489A>G XP_011531289.1:n.-99-489A>G
XM_017004503.1:c.-183-405A>G XP_016859992.1:n.-183-405A>G
NM_001135651.3:c.-183-405A>G MANE Select NP_001129123.1:n.-183-405A>G
NM_002759.4:c.-417-171A>G NP_002750.1:n.-417-171A>G