Canonical Allele Identifier: CA425409783
Gene: EIF2B4 HGNC NCBI
GTF3C2-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27364525G>T , CM000664.2:g.27364525G>T GRCh38
NC_000002.11:g.27587392G>T , CM000664.1:g.27587392G>T GRCh37
NC_000002.10:g.27440896G>T NCBI36
NG_009305.1:g.10933C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000347454.9:c.1447C>A (EIF2B4) MANE Select ENSP00000233552.6:p.Arg483=
ENST00000347454.8:c.1447C>A (EIF2B4) ENSP00000233552.5:p.Arg483=
ENST00000405940.6:c.*713C>A (EIF2B4) ENSP00000384375.2:n.*713C>A
ENST00000445933.6:c.1444C>A (EIF2B4) ENSP00000394397.2:p.Arg482=
ENST00000451130.6:c.1507C>A (EIF2B4) ENSP00000394869.2:p.Arg503=
ENST00000478311.1:n.440C>A (EIF2B4)
ENST00000493344.6:c.1510C>A (EIF2B4) ENSP00000429323.1:p.Arg504=
ENST00000616081.4:c.1438C>A (EIF2B4) ENSP00000477710.1:p.Arg480=
ENST00000622434.4:c.*713C>A (EIF2B4) ENSP00000479991.1:n.*713C>A
NM_001034116.1:c.1447C>A (EIF2B4) NP_001029288.1:p.Arg483=
NM_015636.3:c.1444C>A (EIF2B4) NP_056451.3:p.Arg482=
NM_172195.3:c.1507C>A (EIF2B4) NP_751945.2:p.Arg503=
XM_005264632.1:c.1402C>A (EIF2B4) XP_005264689.1:p.Arg468=
XM_006712132.1:c.1399C>A (EIF2B4) XP_006712195.1:p.Arg467=
XM_011533147.1:c.829C>A (EIF2B4) XP_011531449.1:p.Arg277=
XR_939868.1:n.1772-2899G>T (GTF3C2-AS2)
NM_001318965.1:c.1510C>A (EIF2B4) NP_001305894.1:p.Arg504=
NM_001318966.1:c.1402C>A (EIF2B4) NP_001305895.1:p.Arg468=
NM_001318967.1:c.1354C>A (EIF2B4) NP_001305896.1:p.Arg452=
NM_001318968.1:c.862C>A (EIF2B4) NP_001305897.1:p.Arg288=
NM_001318969.1:c.829C>A (EIF2B4) NP_001305898.1:p.Arg277=
XM_011533147.2:c.829C>A (EIF2B4) XP_011531449.1:p.Arg277=
NM_001034116.2:c.1447C>A (EIF2B4) MANE Select NP_001029288.1:p.Arg483=
NM_001318965.2:c.1510C>A (EIF2B4) NP_001305894.1:p.Arg504=
NM_001318966.2:c.1402C>A (EIF2B4) NP_001305895.1:p.Arg468=
NM_001318967.2:c.1354C>A (EIF2B4) NP_001305896.1:p.Arg452=
NM_001318968.2:c.862C>A (EIF2B4) NP_001305897.1:p.Arg288=
NM_001318969.2:c.829C>A (EIF2B4) NP_001305898.1:p.Arg277=
NM_015636.4:c.1444C>A (EIF2B4) NP_056451.3:p.Arg482=
NM_172195.4:c.1507C>A (EIF2B4) NP_751945.2:p.Arg503=