Canonical Allele Identifier: CA346197467

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27589634G>C (hg19) ; chr2:g.27366767G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27366767G>C , CM000664.2:g.27366767G>C	GRCh38
NC_000002.11:g.27589634G>C , CM000664.1:g.27589634G>C	GRCh37
NC_000002.10:g.27443138G>C	NCBI36
NG_009305.1:g.8691C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000347454.9:c.1183C>G (EIF2B4) MANE Select	ENSP00000233552.6:p.Leu395Val
ENST00000347454.8:c.1183C>G (EIF2B4)	ENSP00000233552.5:p.Leu395Val
ENST00000405940.6:c.*449C>G (EIF2B4)	ENSP00000384375.2:n.*449C>G
ENST00000417567.1:c.757C>G (EIF2B4)
ENST00000445933.6:c.1180C>G (EIF2B4)	ENSP00000394397.2:p.Leu394Val
ENST00000451130.6:c.1243C>G (EIF2B4)	ENSP00000394869.2:p.Leu415Val
ENST00000475582.5:n.3084C>G (EIF2B4)
ENST00000493344.6:c.1246C>G (EIF2B4)	ENSP00000429323.1:p.Leu416Val
ENST00000616081.4:c.1174C>G (EIF2B4)	ENSP00000477710.1:p.Leu392Val
ENST00000622434.4:c.*449C>G (EIF2B4)	ENSP00000479991.1:n.*449C>G
NM_001034116.1:c.1183C>G (EIF2B4)	NP_001029288.1:p.Leu395Val
NM_015636.3:c.1180C>G (EIF2B4)	NP_056451.3:p.Leu394Val
NM_172195.3:c.1243C>G (EIF2B4)	NP_751945.2:p.Leu415Val
XM_005264632.1:c.1138C>G (EIF2B4)	XP_005264689.1:p.Leu380Val
XM_006712132.1:c.1135C>G (EIF2B4)	XP_006712195.1:p.Leu379Val
XM_011533147.1:c.565C>G (EIF2B4)	XP_011531449.1:p.Leu189Val
XR_939868.1:n.1772-657G>C (GTF3C2-AS2)
NM_001318965.1:c.1246C>G (EIF2B4)	NP_001305894.1:p.Leu416Val
NM_001318966.1:c.1138C>G (EIF2B4)	NP_001305895.1:p.Leu380Val
NM_001318967.1:c.1090C>G (EIF2B4)	NP_001305896.1:p.Leu364Val
NM_001318968.1:c.598C>G (EIF2B4)	NP_001305897.1:p.Leu200Val
NM_001318969.1:c.565C>G (EIF2B4)	NP_001305898.1:p.Leu189Val
XM_011533147.2:c.565C>G (EIF2B4)	XP_011531449.1:p.Leu189Val
NM_001034116.2:c.1183C>G (EIF2B4) MANE Select	NP_001029288.1:p.Leu395Val
NM_001318965.2:c.1246C>G (EIF2B4)	NP_001305894.1:p.Leu416Val
NM_001318966.2:c.1138C>G (EIF2B4)	NP_001305895.1:p.Leu380Val
NM_001318967.2:c.1090C>G (EIF2B4)	NP_001305896.1:p.Leu364Val
NM_001318968.2:c.598C>G (EIF2B4)	NP_001305897.1:p.Leu200Val
NM_001318969.2:c.565C>G (EIF2B4)	NP_001305898.1:p.Leu189Val
NM_015636.4:c.1180C>G (EIF2B4)	NP_056451.3:p.Leu394Val
NM_172195.4:c.1243C>G (EIF2B4)	NP_751945.2:p.Leu415Val