Canonical Allele Identifier: CA346197464
Gene: EIF2B4 HGNC NCBI
GTF3C2-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27366766A>G , CM000664.2:g.27366766A>G GRCh38
NC_000002.11:g.27589633A>G , CM000664.1:g.27589633A>G GRCh37
NC_000002.10:g.27443137A>G NCBI36
NG_009305.1:g.8692T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000347454.9:c.1184T>C (EIF2B4) MANE Select ENSP00000233552.6:p.Leu395Pro
ENST00000347454.8:c.1184T>C (EIF2B4) ENSP00000233552.5:p.Leu395Pro
ENST00000405940.6:c.*450T>C (EIF2B4) ENSP00000384375.2:n.*450T>C
ENST00000417567.1:c.758T>C (EIF2B4)
ENST00000445933.6:c.1181T>C (EIF2B4) ENSP00000394397.2:p.Leu394Pro
ENST00000451130.6:c.1244T>C (EIF2B4) ENSP00000394869.2:p.Leu415Pro
ENST00000475582.5:n.3085T>C (EIF2B4)
ENST00000493344.6:c.1247T>C (EIF2B4) ENSP00000429323.1:p.Leu416Pro
ENST00000616081.4:c.1175T>C (EIF2B4) ENSP00000477710.1:p.Leu392Pro
ENST00000622434.4:c.*450T>C (EIF2B4) ENSP00000479991.1:n.*450T>C
NM_001034116.1:c.1184T>C (EIF2B4) NP_001029288.1:p.Leu395Pro
NM_015636.3:c.1181T>C (EIF2B4) NP_056451.3:p.Leu394Pro
NM_172195.3:c.1244T>C (EIF2B4) NP_751945.2:p.Leu415Pro
XM_005264632.1:c.1139T>C (EIF2B4) XP_005264689.1:p.Leu380Pro
XM_006712132.1:c.1136T>C (EIF2B4) XP_006712195.1:p.Leu379Pro
XM_011533147.1:c.566T>C (EIF2B4) XP_011531449.1:p.Leu189Pro
XR_939868.1:n.1772-658A>G (GTF3C2-AS2)
NM_001318965.1:c.1247T>C (EIF2B4) NP_001305894.1:p.Leu416Pro
NM_001318966.1:c.1139T>C (EIF2B4) NP_001305895.1:p.Leu380Pro
NM_001318967.1:c.1091T>C (EIF2B4) NP_001305896.1:p.Leu364Pro
NM_001318968.1:c.599T>C (EIF2B4) NP_001305897.1:p.Leu200Pro
NM_001318969.1:c.566T>C (EIF2B4) NP_001305898.1:p.Leu189Pro
XM_011533147.2:c.566T>C (EIF2B4) XP_011531449.1:p.Leu189Pro
NM_001034116.2:c.1184T>C (EIF2B4) MANE Select NP_001029288.1:p.Leu395Pro
NM_001318965.2:c.1247T>C (EIF2B4) NP_001305894.1:p.Leu416Pro
NM_001318966.2:c.1139T>C (EIF2B4) NP_001305895.1:p.Leu380Pro
NM_001318967.2:c.1091T>C (EIF2B4) NP_001305896.1:p.Leu364Pro
NM_001318968.2:c.599T>C (EIF2B4) NP_001305897.1:p.Leu200Pro
NM_001318969.2:c.566T>C (EIF2B4) NP_001305898.1:p.Leu189Pro
NM_015636.4:c.1181T>C (EIF2B4) NP_056451.3:p.Leu394Pro
NM_172195.4:c.1244T>C (EIF2B4) NP_751945.2:p.Leu415Pro