Canonical Allele Identifier: CA346196870

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587603A>T (hg19) ; chr2:g.27364736A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364736A>T , CM000664.2:g.27364736A>T	GRCh38
NC_000002.11:g.27587603A>T , CM000664.1:g.27587603A>T	GRCh37
NC_000002.10:g.27441107A>T	NCBI36
NG_009305.1:g.10722T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1354T>A (EIF2B4) MANE Select	ENSP00000233552.6:p.Phe452Ile
ENST00000347454.8:c.1354T>A (EIF2B4)	ENSP00000233552.5:p.Phe452Ile
ENST00000405940.6:c.*620T>A (EIF2B4)	ENSP00000384375.2:n.*620T>A
ENST00000445933.6:c.1351T>A (EIF2B4)	ENSP00000394397.2:p.Phe451Ile
ENST00000451130.6:c.1414T>A (EIF2B4)	ENSP00000394869.2:p.Phe472Ile
ENST00000478311.1:n.347T>A (EIF2B4)
ENST00000493344.6:c.1417T>A (EIF2B4)	ENSP00000429323.1:p.Phe473Ile
ENST00000616081.4:c.1345T>A (EIF2B4)	ENSP00000477710.1:p.Phe449Ile
ENST00000622434.4:c.*620T>A (EIF2B4)	ENSP00000479991.1:n.*620T>A
NM_001034116.1:c.1354T>A (EIF2B4)	NP_001029288.1:p.Phe452Ile
NM_015636.3:c.1351T>A (EIF2B4)	NP_056451.3:p.Phe451Ile
NM_172195.3:c.1414T>A (EIF2B4)	NP_751945.2:p.Phe472Ile
XM_005264632.1:c.1309T>A (EIF2B4)	XP_005264689.1:p.Phe437Ile
XM_006712132.1:c.1306T>A (EIF2B4)	XP_006712195.1:p.Phe436Ile
XM_011533147.1:c.736T>A (EIF2B4)	XP_011531449.1:p.Phe246Ile
XR_939868.1:n.1772-2688A>T (GTF3C2-AS2)
NM_001318965.1:c.1417T>A (EIF2B4)	NP_001305894.1:p.Phe473Ile
NM_001318966.1:c.1309T>A (EIF2B4)	NP_001305895.1:p.Phe437Ile
NM_001318967.1:c.1261T>A (EIF2B4)	NP_001305896.1:p.Phe421Ile
NM_001318968.1:c.769T>A (EIF2B4)	NP_001305897.1:p.Phe257Ile
NM_001318969.1:c.736T>A (EIF2B4)	NP_001305898.1:p.Phe246Ile
XM_011533147.2:c.736T>A (EIF2B4)	XP_011531449.1:p.Phe246Ile
NM_001034116.2:c.1354T>A (EIF2B4) MANE Select	NP_001029288.1:p.Phe452Ile
NM_001318965.2:c.1417T>A (EIF2B4)	NP_001305894.1:p.Phe473Ile
NM_001318966.2:c.1309T>A (EIF2B4)	NP_001305895.1:p.Phe437Ile
NM_001318967.2:c.1261T>A (EIF2B4)	NP_001305896.1:p.Phe421Ile
NM_001318968.2:c.769T>A (EIF2B4)	NP_001305897.1:p.Phe257Ile
NM_001318969.2:c.736T>A (EIF2B4)	NP_001305898.1:p.Phe246Ile
NM_015636.4:c.1351T>A (EIF2B4)	NP_056451.3:p.Phe451Ile
NM_172195.4:c.1414T>A (EIF2B4)	NP_751945.2:p.Phe472Ile