Canonical Allele Identifier: CA2586968819
Gene: EIF2B4 HGNC NCBI
GTF3C2-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27364718dup , CM000664.2:g.27364718dup GRCh38
NC_000002.11:g.27587585dup , CM000664.1:g.27587585dup GRCh37
NC_000002.10:g.27441089dup NCBI36
NG_009305.1:g.10741dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000347454.9:c.1372+1dup (EIF2B4)
ENST00000347454.8:c.1372+1dup (EIF2B4)
ENST00000405940.6:c.*638+1dup (EIF2B4)
ENST00000445933.6:c.1369+1dup (EIF2B4)
ENST00000451130.6:c.1432+1dup (EIF2B4)
ENST00000478311.1:n.365+1dup (EIF2B4)
ENST00000493344.6:c.1435+1dup (EIF2B4)
ENST00000616081.4:c.1363+1dup (EIF2B4)
ENST00000622434.4:c.*638+1dup (EIF2B4)
NM_001034116.1:c.1372+1dup (EIF2B4)
NM_015636.3:c.1369+1dup (EIF2B4)
NM_172195.3:c.1432+1dup (EIF2B4)
XM_005264632.1:c.1327+1dup (EIF2B4)
XM_006712132.1:c.1324+1dup (EIF2B4)
XM_011533147.1:c.754+1dup (EIF2B4)
XR_939868.1:n.1772-2706dup (GTF3C2-AS2)
NM_001318965.1:c.1435+1dup (EIF2B4)
NM_001318966.1:c.1327+1dup (EIF2B4)
NM_001318967.1:c.1279+1dup (EIF2B4)
NM_001318968.1:c.787+1dup (EIF2B4)
NM_001318969.1:c.754+1dup (EIF2B4)
XM_011533147.2:c.754+1dup (EIF2B4)
NM_001034116.2:c.1372+1dup (EIF2B4)
NM_001318965.2:c.1435+1dup (EIF2B4)
NM_001318966.2:c.1327+1dup (EIF2B4)
NM_001318967.2:c.1279+1dup (EIF2B4)
NM_001318968.2:c.787+1dup (EIF2B4)
NM_001318969.2:c.754+1dup (EIF2B4)
NM_015636.4:c.1369+1dup (EIF2B4)
NM_172195.4:c.1432+1dup (EIF2B4)