Canonical Allele Identifier: CA346197367

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587755A>G (hg19) ; chr2:g.27364888A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364888A>G , CM000664.2:g.27364888A>G	GRCh38
NC_000002.11:g.27587755A>G , CM000664.1:g.27587755A>G	GRCh37
NC_000002.10:g.27441259A>G	NCBI36
NG_009305.1:g.10570T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1202T>C (EIF2B4) MANE Select	ENSP00000233552.6:p.Val401Ala
ENST00000347454.8:c.1202T>C (EIF2B4)	ENSP00000233552.5:p.Val401Ala
ENST00000405940.6:c.*468T>C (EIF2B4)	ENSP00000384375.2:n.*468T>C
ENST00000445933.6:c.1199T>C (EIF2B4)	ENSP00000394397.2:p.Val400Ala
ENST00000451130.6:c.1262T>C (EIF2B4)	ENSP00000394869.2:p.Val421Ala
ENST00000478311.1:n.195T>C (EIF2B4)
ENST00000493344.6:c.1265T>C (EIF2B4)	ENSP00000429323.1:p.Val422Ala
ENST00000616081.4:c.1193T>C (EIF2B4)	ENSP00000477710.1:p.Val398Ala
ENST00000622434.4:c.*468T>C (EIF2B4)	ENSP00000479991.1:n.*468T>C
NM_001034116.1:c.1202T>C (EIF2B4)	NP_001029288.1:p.Val401Ala
NM_015636.3:c.1199T>C (EIF2B4)	NP_056451.3:p.Val400Ala
NM_172195.3:c.1262T>C (EIF2B4)	NP_751945.2:p.Val421Ala
XM_005264632.1:c.1157T>C (EIF2B4)	XP_005264689.1:p.Val386Ala
XM_006712132.1:c.1154T>C (EIF2B4)	XP_006712195.1:p.Val385Ala
XM_011533147.1:c.584T>C (EIF2B4)	XP_011531449.1:p.Val195Ala
XR_939868.1:n.1772-2536A>G (GTF3C2-AS2)
NM_001318965.1:c.1265T>C (EIF2B4)	NP_001305894.1:p.Val422Ala
NM_001318966.1:c.1157T>C (EIF2B4)	NP_001305895.1:p.Val386Ala
NM_001318967.1:c.1109T>C (EIF2B4)	NP_001305896.1:p.Val370Ala
NM_001318968.1:c.617T>C (EIF2B4)	NP_001305897.1:p.Val206Ala
NM_001318969.1:c.584T>C (EIF2B4)	NP_001305898.1:p.Val195Ala
XM_011533147.2:c.584T>C (EIF2B4)	XP_011531449.1:p.Val195Ala
NM_001034116.2:c.1202T>C (EIF2B4) MANE Select	NP_001029288.1:p.Val401Ala
NM_001318965.2:c.1265T>C (EIF2B4)	NP_001305894.1:p.Val422Ala
NM_001318966.2:c.1157T>C (EIF2B4)	NP_001305895.1:p.Val386Ala
NM_001318967.2:c.1109T>C (EIF2B4)	NP_001305896.1:p.Val370Ala
NM_001318968.2:c.617T>C (EIF2B4)	NP_001305897.1:p.Val206Ala
NM_001318969.2:c.584T>C (EIF2B4)	NP_001305898.1:p.Val195Ala
NM_015636.4:c.1199T>C (EIF2B4)	NP_056451.3:p.Val400Ala
NM_172195.4:c.1262T>C (EIF2B4)	NP_751945.2:p.Val421Ala