Canonical Allele Identifier: CA346196959

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587629A>T (hg19) ; chr2:g.27364762A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364762A>T , CM000664.2:g.27364762A>T	GRCh38
NC_000002.11:g.27587629A>T , CM000664.1:g.27587629A>T	GRCh37
NC_000002.10:g.27441133A>T	NCBI36
NG_009305.1:g.10696T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1328T>A (EIF2B4) MANE Select	ENSP00000233552.6:p.Phe443Tyr
ENST00000347454.8:c.1328T>A (EIF2B4)	ENSP00000233552.5:p.Phe443Tyr
ENST00000405940.6:c.*594T>A (EIF2B4)	ENSP00000384375.2:n.*594T>A
ENST00000445933.6:c.1325T>A (EIF2B4)	ENSP00000394397.2:p.Phe442Tyr
ENST00000451130.6:c.1388T>A (EIF2B4)	ENSP00000394869.2:p.Phe463Tyr
ENST00000478311.1:n.321T>A (EIF2B4)
ENST00000493344.6:c.1391T>A (EIF2B4)	ENSP00000429323.1:p.Phe464Tyr
ENST00000616081.4:c.1319T>A (EIF2B4)	ENSP00000477710.1:p.Phe440Tyr
ENST00000622434.4:c.*594T>A (EIF2B4)	ENSP00000479991.1:n.*594T>A
NM_001034116.1:c.1328T>A (EIF2B4)	NP_001029288.1:p.Phe443Tyr
NM_015636.3:c.1325T>A (EIF2B4)	NP_056451.3:p.Phe442Tyr
NM_172195.3:c.1388T>A (EIF2B4)	NP_751945.2:p.Phe463Tyr
XM_005264632.1:c.1283T>A (EIF2B4)	XP_005264689.1:p.Phe428Tyr
XM_006712132.1:c.1280T>A (EIF2B4)	XP_006712195.1:p.Phe427Tyr
XM_011533147.1:c.710T>A (EIF2B4)	XP_011531449.1:p.Phe237Tyr
XR_939868.1:n.1772-2662A>T (GTF3C2-AS2)
NM_001318965.1:c.1391T>A (EIF2B4)	NP_001305894.1:p.Phe464Tyr
NM_001318966.1:c.1283T>A (EIF2B4)	NP_001305895.1:p.Phe428Tyr
NM_001318967.1:c.1235T>A (EIF2B4)	NP_001305896.1:p.Phe412Tyr
NM_001318968.1:c.743T>A (EIF2B4)	NP_001305897.1:p.Phe248Tyr
NM_001318969.1:c.710T>A (EIF2B4)	NP_001305898.1:p.Phe237Tyr
XM_011533147.2:c.710T>A (EIF2B4)	XP_011531449.1:p.Phe237Tyr
NM_001034116.2:c.1328T>A (EIF2B4) MANE Select	NP_001029288.1:p.Phe443Tyr
NM_001318965.2:c.1391T>A (EIF2B4)	NP_001305894.1:p.Phe464Tyr
NM_001318966.2:c.1283T>A (EIF2B4)	NP_001305895.1:p.Phe428Tyr
NM_001318967.2:c.1235T>A (EIF2B4)	NP_001305896.1:p.Phe412Tyr
NM_001318968.2:c.743T>A (EIF2B4)	NP_001305897.1:p.Phe248Tyr
NM_001318969.2:c.710T>A (EIF2B4)	NP_001305898.1:p.Phe237Tyr
NM_015636.4:c.1325T>A (EIF2B4)	NP_056451.3:p.Phe442Tyr
NM_172195.4:c.1388T>A (EIF2B4)	NP_751945.2:p.Phe463Tyr