Canonical Allele Identifier: CA1245139382
Gene: EIF2AK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.37149501T= , CM000664.2:g.37149501T= GRCh38
NC_000002.11:g.37376644T= , CM000664.1:g.37376644T= GRCh37
NC_000002.10:g.37230148T= NCBI36
NG_030351.1:g.12547A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233057.9:c.-183-478A= MANE Select ENSP00000233057.4:n.-183-478A=
ENST00000411537.7:n.29-478A=
ENST00000679507.1:c.-16-1679A= ENSP00000506024.1:n.-16-1679A=
ENST00000679979.1:c.-183-478A= ENSP00000506455.1:n.-183-478A=
ENST00000680273.1:c.-183-478A= ENSP00000506203.1:n.-183-478A=
ENST00000681329.1:n.157-478A=
ENST00000681463.1:c.-75-586A= ENSP00000505138.1:n.-75-586A=
ENST00000681507.1:c.-99-562A= ENSP00000505772.1:n.-99-562A=
ENST00000233057.8:c.-183-478A= ENSP00000233057.4:n.-183-478A=
ENST00000390013.3:c.-99-562A= ENSP00000374663.3:n.-99-562A=
ENST00000395127.6:c.-417-244A= ENSP00000378559.2:n.-417-244A=
ENST00000411537.6:c.-75-586A= ENSP00000393921.2:n.-75-586A=
NM_001135651.2:c.-183-478A= NP_001129123.1:n.-183-478A=
NM_002759.3:c.-417-244A= NP_002750.1:n.-417-244A=
XM_011532987.1:c.-99-562A= XP_011531289.1:n.-99-562A=
XM_011532987.2:c.-99-562A= XP_011531289.1:n.-99-562A=
XM_017004503.1:c.-183-478A= XP_016859992.1:n.-183-478A=
NM_001135651.3:c.-183-478A= MANE Select NP_001129123.1:n.-183-478A=
NM_002759.4:c.-417-244A= NP_002750.1:n.-417-244A=