Canonical Allele Identifier: CA346197405
Gene: EIF2B4 HGNC NCBI
GTF3C2-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27364897A>C , CM000664.2:g.27364897A>C GRCh38
NC_000002.11:g.27587764A>C , CM000664.1:g.27587764A>C GRCh37
NC_000002.10:g.27441268A>C NCBI36
NG_009305.1:g.10561T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000347454.9:c.1193T>G (EIF2B4) MANE Select ENSP00000233552.6:p.Val398Gly
ENST00000347454.8:c.1193T>G (EIF2B4) ENSP00000233552.5:p.Val398Gly
ENST00000405940.6:c.*459T>G (EIF2B4) ENSP00000384375.2:n.*459T>G
ENST00000445933.6:c.1190T>G (EIF2B4) ENSP00000394397.2:p.Val397Gly
ENST00000451130.6:c.1253T>G (EIF2B4) ENSP00000394869.2:p.Val418Gly
ENST00000478311.1:n.186T>G (EIF2B4)
ENST00000493344.6:c.1256T>G (EIF2B4) ENSP00000429323.1:p.Val419Gly
ENST00000616081.4:c.1184T>G (EIF2B4) ENSP00000477710.1:p.Val395Gly
ENST00000622434.4:c.*459T>G (EIF2B4) ENSP00000479991.1:n.*459T>G
NM_001034116.1:c.1193T>G (EIF2B4) NP_001029288.1:p.Val398Gly
NM_015636.3:c.1190T>G (EIF2B4) NP_056451.3:p.Val397Gly
NM_172195.3:c.1253T>G (EIF2B4) NP_751945.2:p.Val418Gly
XM_005264632.1:c.1148T>G (EIF2B4) XP_005264689.1:p.Val383Gly
XM_006712132.1:c.1145T>G (EIF2B4) XP_006712195.1:p.Val382Gly
XM_011533147.1:c.575T>G (EIF2B4) XP_011531449.1:p.Val192Gly
XR_939868.1:n.1772-2527A>C (GTF3C2-AS2)
NM_001318965.1:c.1256T>G (EIF2B4) NP_001305894.1:p.Val419Gly
NM_001318966.1:c.1148T>G (EIF2B4) NP_001305895.1:p.Val383Gly
NM_001318967.1:c.1100T>G (EIF2B4) NP_001305896.1:p.Val367Gly
NM_001318968.1:c.608T>G (EIF2B4) NP_001305897.1:p.Val203Gly
NM_001318969.1:c.575T>G (EIF2B4) NP_001305898.1:p.Val192Gly
XM_011533147.2:c.575T>G (EIF2B4) XP_011531449.1:p.Val192Gly
NM_001034116.2:c.1193T>G (EIF2B4) MANE Select NP_001029288.1:p.Val398Gly
NM_001318965.2:c.1256T>G (EIF2B4) NP_001305894.1:p.Val419Gly
NM_001318966.2:c.1148T>G (EIF2B4) NP_001305895.1:p.Val383Gly
NM_001318967.2:c.1100T>G (EIF2B4) NP_001305896.1:p.Val367Gly
NM_001318968.2:c.608T>G (EIF2B4) NP_001305897.1:p.Val203Gly
NM_001318969.2:c.575T>G (EIF2B4) NP_001305898.1:p.Val192Gly
NM_015636.4:c.1190T>G (EIF2B4) NP_056451.3:p.Val397Gly
NM_172195.4:c.1253T>G (EIF2B4) NP_751945.2:p.Val418Gly