Canonical Allele Identifier: CA1245139387
Gene: EIF2AK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.37149513G= , CM000664.2:g.37149513G= GRCh38
NC_000002.11:g.37376656G= , CM000664.1:g.37376656G= GRCh37
NC_000002.10:g.37230160G= NCBI36
NG_030351.1:g.12535C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233057.9:c.-183-490C= MANE Select ENSP00000233057.4:n.-183-490C=
ENST00000411537.7:n.29-490C=
ENST00000679507.1:c.-16-1691C= ENSP00000506024.1:n.-16-1691C=
ENST00000679979.1:c.-183-490C= ENSP00000506455.1:n.-183-490C=
ENST00000680273.1:c.-183-490C= ENSP00000506203.1:n.-183-490C=
ENST00000681329.1:n.157-490C=
ENST00000681463.1:c.-75-598C= ENSP00000505138.1:n.-75-598C=
ENST00000681507.1:c.-99-574C= ENSP00000505772.1:n.-99-574C=
ENST00000233057.8:c.-183-490C= ENSP00000233057.4:n.-183-490C=
ENST00000390013.3:c.-99-574C= ENSP00000374663.3:n.-99-574C=
ENST00000395127.6:c.-417-256C= ENSP00000378559.2:n.-417-256C=
ENST00000411537.6:c.-75-598C= ENSP00000393921.2:n.-75-598C=
NM_001135651.2:c.-183-490C= NP_001129123.1:n.-183-490C=
NM_002759.3:c.-417-256C= NP_002750.1:n.-417-256C=
XM_011532987.1:c.-99-574C= XP_011531289.1:n.-99-574C=
XM_011532987.2:c.-99-574C= XP_011531289.1:n.-99-574C=
XM_017004503.1:c.-183-490C= XP_016859992.1:n.-183-490C=
NM_001135651.3:c.-183-490C= MANE Select NP_001129123.1:n.-183-490C=
NM_002759.4:c.-417-256C= NP_002750.1:n.-417-256C=