Canonical Allele Identifier: CA346196933

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587623T>A (hg19) ; chr2:g.27364756T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364756T>A , CM000664.2:g.27364756T>A	GRCh38
NC_000002.11:g.27587623T>A , CM000664.1:g.27587623T>A	GRCh37
NC_000002.10:g.27441127T>A	NCBI36
NG_009305.1:g.10702A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1334A>T (EIF2B4) MANE Select	ENSP00000233552.6:p.Glu445Val
ENST00000347454.8:c.1334A>T (EIF2B4)	ENSP00000233552.5:p.Glu445Val
ENST00000405940.6:c.*600A>T (EIF2B4)	ENSP00000384375.2:n.*600A>T
ENST00000445933.6:c.1331A>T (EIF2B4)	ENSP00000394397.2:p.Glu444Val
ENST00000451130.6:c.1394A>T (EIF2B4)	ENSP00000394869.2:p.Glu465Val
ENST00000478311.1:n.327A>T (EIF2B4)
ENST00000493344.6:c.1397A>T (EIF2B4)	ENSP00000429323.1:p.Glu466Val
ENST00000616081.4:c.1325A>T (EIF2B4)	ENSP00000477710.1:p.Glu442Val
ENST00000622434.4:c.*600A>T (EIF2B4)	ENSP00000479991.1:n.*600A>T
NM_001034116.1:c.1334A>T (EIF2B4)	NP_001029288.1:p.Glu445Val
NM_015636.3:c.1331A>T (EIF2B4)	NP_056451.3:p.Glu444Val
NM_172195.3:c.1394A>T (EIF2B4)	NP_751945.2:p.Glu465Val
XM_005264632.1:c.1289A>T (EIF2B4)	XP_005264689.1:p.Glu430Val
XM_006712132.1:c.1286A>T (EIF2B4)	XP_006712195.1:p.Glu429Val
XM_011533147.1:c.716A>T (EIF2B4)	XP_011531449.1:p.Glu239Val
XR_939868.1:n.1772-2668T>A (GTF3C2-AS2)
NM_001318965.1:c.1397A>T (EIF2B4)	NP_001305894.1:p.Glu466Val
NM_001318966.1:c.1289A>T (EIF2B4)	NP_001305895.1:p.Glu430Val
NM_001318967.1:c.1241A>T (EIF2B4)	NP_001305896.1:p.Glu414Val
NM_001318968.1:c.749A>T (EIF2B4)	NP_001305897.1:p.Glu250Val
NM_001318969.1:c.716A>T (EIF2B4)	NP_001305898.1:p.Glu239Val
XM_011533147.2:c.716A>T (EIF2B4)	XP_011531449.1:p.Glu239Val
NM_001034116.2:c.1334A>T (EIF2B4) MANE Select	NP_001029288.1:p.Glu445Val
NM_001318965.2:c.1397A>T (EIF2B4)	NP_001305894.1:p.Glu466Val
NM_001318966.2:c.1289A>T (EIF2B4)	NP_001305895.1:p.Glu430Val
NM_001318967.2:c.1241A>T (EIF2B4)	NP_001305896.1:p.Glu414Val
NM_001318968.2:c.749A>T (EIF2B4)	NP_001305897.1:p.Glu250Val
NM_001318969.2:c.716A>T (EIF2B4)	NP_001305898.1:p.Glu239Val
NM_015636.4:c.1331A>T (EIF2B4)	NP_056451.3:p.Glu444Val
NM_172195.4:c.1394A>T (EIF2B4)	NP_751945.2:p.Glu465Val