Canonical Allele Identifier: CA346197075

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587663C>T (hg19) ; chr2:g.27364796C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364796C>T , CM000664.2:g.27364796C>T	GRCh38
NC_000002.11:g.27587663C>T , CM000664.1:g.27587663C>T	GRCh37
NC_000002.10:g.27441167C>T	NCBI36
NG_009305.1:g.10662G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1294G>A (EIF2B4) MANE Select	ENSP00000233552.6:p.Val432Ile
ENST00000347454.8:c.1294G>A (EIF2B4)	ENSP00000233552.5:p.Val432Ile
ENST00000405940.6:c.*560G>A (EIF2B4)	ENSP00000384375.2:n.*560G>A
ENST00000445933.6:c.1291G>A (EIF2B4)	ENSP00000394397.2:p.Val431Ile
ENST00000451130.6:c.1354G>A (EIF2B4)	ENSP00000394869.2:p.Val452Ile
ENST00000478311.1:n.287G>A (EIF2B4)
ENST00000493344.6:c.1357G>A (EIF2B4)	ENSP00000429323.1:p.Val453Ile
ENST00000616081.4:c.1285G>A (EIF2B4)	ENSP00000477710.1:p.Val429Ile
ENST00000622434.4:c.*560G>A (EIF2B4)	ENSP00000479991.1:n.*560G>A
NM_001034116.1:c.1294G>A (EIF2B4)	NP_001029288.1:p.Val432Ile
NM_015636.3:c.1291G>A (EIF2B4)	NP_056451.3:p.Val431Ile
NM_172195.3:c.1354G>A (EIF2B4)	NP_751945.2:p.Val452Ile
XM_005264632.1:c.1249G>A (EIF2B4)	XP_005264689.1:p.Val417Ile
XM_006712132.1:c.1246G>A (EIF2B4)	XP_006712195.1:p.Val416Ile
XM_011533147.1:c.676G>A (EIF2B4)	XP_011531449.1:p.Val226Ile
XR_939868.1:n.1772-2628C>T (GTF3C2-AS2)
NM_001318965.1:c.1357G>A (EIF2B4)	NP_001305894.1:p.Val453Ile
NM_001318966.1:c.1249G>A (EIF2B4)	NP_001305895.1:p.Val417Ile
NM_001318967.1:c.1201G>A (EIF2B4)	NP_001305896.1:p.Val401Ile
NM_001318968.1:c.709G>A (EIF2B4)	NP_001305897.1:p.Val237Ile
NM_001318969.1:c.676G>A (EIF2B4)	NP_001305898.1:p.Val226Ile
XM_011533147.2:c.676G>A (EIF2B4)	XP_011531449.1:p.Val226Ile
NM_001034116.2:c.1294G>A (EIF2B4) MANE Select	NP_001029288.1:p.Val432Ile
NM_001318965.2:c.1357G>A (EIF2B4)	NP_001305894.1:p.Val453Ile
NM_001318966.2:c.1249G>A (EIF2B4)	NP_001305895.1:p.Val417Ile
NM_001318967.2:c.1201G>A (EIF2B4)	NP_001305896.1:p.Val401Ile
NM_001318968.2:c.709G>A (EIF2B4)	NP_001305897.1:p.Val237Ile
NM_001318969.2:c.676G>A (EIF2B4)	NP_001305898.1:p.Val226Ile
NM_015636.4:c.1291G>A (EIF2B4)	NP_056451.3:p.Val431Ile
NM_172195.4:c.1354G>A (EIF2B4)	NP_751945.2:p.Val452Ile