Canonical Allele Identifier: CA1245139269
Gene: EIF2AK2 HGNC NCBI
ARL14EPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.37149257A= , CM000664.2:g.37149257A= GRCh38
NC_000002.11:g.37376400A= , CM000664.1:g.37376400A= GRCh37
NC_000002.10:g.37229904A= NCBI36
NG_030351.1:g.12791T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233057.9:c.-183-234T= (EIF2AK2) MANE Select ENSP00000233057.4:n.-183-234T=
ENST00000411537.7:n.29-234T= (EIF2AK2)
ENST00000679507.1:c.-16-1435T= (EIF2AK2) ENSP00000506024.1:n.-16-1435T=
ENST00000679979.1:c.-183-234T= (EIF2AK2) ENSP00000506455.1:n.-183-234T=
ENST00000680273.1:c.-183-234T= (EIF2AK2) ENSP00000506203.1:n.-183-234T=
ENST00000681329.1:n.157-234T= (EIF2AK2)
ENST00000681463.1:c.-75-342T= (EIF2AK2) ENSP00000505138.1:n.-75-342T=
ENST00000681507.1:c.-99-318T= (EIF2AK2) ENSP00000505772.1:n.-99-318T=
ENST00000233057.8:c.-183-234T= (EIF2AK2) ENSP00000233057.4:n.-183-234T=
ENST00000390013.3:c.-99-318T= (EIF2AK2) ENSP00000374663.3:n.-99-318T=
ENST00000395127.6:c.-417T= (EIF2AK2) ENSP00000378559.2:n.-417T=
ENST00000411537.6:c.-75-342T= (EIF2AK2) ENSP00000393921.2:n.-75-342T=
ENST00000412776.1:n.728A= (ARL14EPP1)
NM_001135651.2:c.-183-234T= (EIF2AK2) NP_001129123.1:n.-183-234T=
NM_002759.3:c.-417T= (EIF2AK2) NP_002750.1:n.-417T=
XM_011532987.1:c.-99-318T= (EIF2AK2) XP_011531289.1:n.-99-318T=
XM_011532987.2:c.-99-318T= (EIF2AK2) XP_011531289.1:n.-99-318T=
XM_017004503.1:c.-183-234T= (EIF2AK2) XP_016859992.1:n.-183-234T=
NM_001135651.3:c.-183-234T= (EIF2AK2) MANE Select NP_001129123.1:n.-183-234T=
NM_002759.4:c.-417T= (EIF2AK2) NP_002750.1:n.-417T=