Canonical Allele Identifier: CA1240244294
Gene: EIF2B4 HGNC NCBI
GTF3C2-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27366734_27366735delinsTG , CM000664.2:g.27366734_27366735delinsTG GRCh38
NC_000002.11:g.27589601_27589602delinsTG , CM000664.1:g.27589601_27589602delinsTG GRCh37
NC_000002.10:g.27443105_27443106delinsTG NCBI36
NG_009305.1:g.8723_8724delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000347454.9:c.1191+24_1191+25delinsCA (EIF2B4) MANE Select ENSP00000233552.6:n.1191+24_1191+25delins...
ENST00000347454.8:c.1191+24_1191+25delinsCA (EIF2B4) ENSP00000233552.5:n.1191+24_1191+25delins...
ENST00000405940.6:c.*457+24_*457+25delinsCA (EIF2B4) ENSP00000384375.2:n.*457+24_*457+25delins...
ENST00000445933.6:c.1188+24_1188+25delinsCA (EIF2B4) ENSP00000394397.2:n.1188+24_1188+25delins...
ENST00000451130.6:c.1251+24_1251+25delinsCA (EIF2B4) ENSP00000394869.2:n.1251+24_1251+25delins...
ENST00000475582.5:n.3116_3117delinsCA (EIF2B4)
ENST00000493344.6:c.1254+24_1254+25delinsCA (EIF2B4) ENSP00000429323.1:n.1254+24_1254+25delins...
ENST00000616081.4:c.1182+24_1182+25delinsCA (EIF2B4) ENSP00000477710.1:n.1182+24_1182+25delins...
ENST00000622434.4:c.*457+24_*457+25delinsCA (EIF2B4) ENSP00000479991.1:n.*457+24_*457+25delins...
NM_001034116.1:c.1191+24_1191+25delinsCA (EIF2B4) NP_001029288.1:n.1191+24_1191+25delinsCA
NM_015636.3:c.1188+24_1188+25delinsCA (EIF2B4) NP_056451.3:n.1188+24_1188+25delinsCA
NM_172195.3:c.1251+24_1251+25delinsCA (EIF2B4) NP_751945.2:n.1251+24_1251+25delinsCA
XM_005264632.1:c.1146+24_1146+25delinsCA (EIF2B4) XP_005264689.1:n.1146+24_1146+25delinsCA
XM_006712132.1:c.1143+24_1143+25delinsCA (EIF2B4) XP_006712195.1:n.1143+24_1143+25delinsCA
XM_011533147.1:c.573+24_573+25delinsCA (EIF2B4) XP_011531449.1:n.573+24_573+25delinsCA
XR_939868.1:n.1772-690_1772-689delinsTG (GTF3C2-AS2)
NM_001318965.1:c.1254+24_1254+25delinsCA (EIF2B4) NP_001305894.1:n.1254+24_1254+25delinsCA
NM_001318966.1:c.1146+24_1146+25delinsCA (EIF2B4) NP_001305895.1:n.1146+24_1146+25delinsCA
NM_001318967.1:c.1098+24_1098+25delinsCA (EIF2B4) NP_001305896.1:n.1098+24_1098+25delinsCA
NM_001318968.1:c.606+24_606+25delinsCA (EIF2B4) NP_001305897.1:n.606+24_606+25delinsCA
NM_001318969.1:c.573+24_573+25delinsCA (EIF2B4) NP_001305898.1:n.573+24_573+25delinsCA
XM_011533147.2:c.573+24_573+25delinsCA (EIF2B4) XP_011531449.1:n.573+24_573+25delinsCA
NM_001034116.2:c.1191+24_1191+25delinsCA (EIF2B4) MANE Select NP_001029288.1:n.1191+24_1191+25delinsCA
NM_001318965.2:c.1254+24_1254+25delinsCA (EIF2B4) NP_001305894.1:n.1254+24_1254+25delinsCA
NM_001318966.2:c.1146+24_1146+25delinsCA (EIF2B4) NP_001305895.1:n.1146+24_1146+25delinsCA
NM_001318967.2:c.1098+24_1098+25delinsCA (EIF2B4) NP_001305896.1:n.1098+24_1098+25delinsCA
NM_001318968.2:c.606+24_606+25delinsCA (EIF2B4) NP_001305897.1:n.606+24_606+25delinsCA
NM_001318969.2:c.573+24_573+25delinsCA (EIF2B4) NP_001305898.1:n.573+24_573+25delinsCA
NM_015636.4:c.1188+24_1188+25delinsCA (EIF2B4) NP_056451.3:n.1188+24_1188+25delinsCA
NM_172195.4:c.1251+24_1251+25delinsCA (EIF2B4) NP_751945.2:n.1251+24_1251+25delinsCA