Canonical Allele Identifier: CA346197178

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587695G>A (hg19) ; chr2:g.27364828G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364828G>A , CM000664.2:g.27364828G>A	GRCh38
NC_000002.11:g.27587695G>A , CM000664.1:g.27587695G>A	GRCh37
NC_000002.10:g.27441199G>A	NCBI36
NG_009305.1:g.10630C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1262C>T (EIF2B4) MANE Select	ENSP00000233552.6:p.Ala421Val
ENST00000347454.8:c.1262C>T (EIF2B4)	ENSP00000233552.5:p.Ala421Val
ENST00000405940.6:c.*528C>T (EIF2B4)	ENSP00000384375.2:n.*528C>T
ENST00000445933.6:c.1259C>T (EIF2B4)	ENSP00000394397.2:p.Ala420Val
ENST00000451130.6:c.1322C>T (EIF2B4)	ENSP00000394869.2:p.Ala441Val
ENST00000478311.1:n.255C>T (EIF2B4)
ENST00000493344.6:c.1325C>T (EIF2B4)	ENSP00000429323.1:p.Ala442Val
ENST00000616081.4:c.1253C>T (EIF2B4)	ENSP00000477710.1:p.Ala418Val
ENST00000622434.4:c.*528C>T (EIF2B4)	ENSP00000479991.1:n.*528C>T
NM_001034116.1:c.1262C>T (EIF2B4)	NP_001029288.1:p.Ala421Val
NM_015636.3:c.1259C>T (EIF2B4)	NP_056451.3:p.Ala420Val
NM_172195.3:c.1322C>T (EIF2B4)	NP_751945.2:p.Ala441Val
XM_005264632.1:c.1217C>T (EIF2B4)	XP_005264689.1:p.Ala406Val
XM_006712132.1:c.1214C>T (EIF2B4)	XP_006712195.1:p.Ala405Val
XM_011533147.1:c.644C>T (EIF2B4)	XP_011531449.1:p.Ala215Val
XR_939868.1:n.1772-2596G>A (GTF3C2-AS2)
NM_001318965.1:c.1325C>T (EIF2B4)	NP_001305894.1:p.Ala442Val
NM_001318966.1:c.1217C>T (EIF2B4)	NP_001305895.1:p.Ala406Val
NM_001318967.1:c.1169C>T (EIF2B4)	NP_001305896.1:p.Ala390Val
NM_001318968.1:c.677C>T (EIF2B4)	NP_001305897.1:p.Ala226Val
NM_001318969.1:c.644C>T (EIF2B4)	NP_001305898.1:p.Ala215Val
XM_011533147.2:c.644C>T (EIF2B4)	XP_011531449.1:p.Ala215Val
NM_001034116.2:c.1262C>T (EIF2B4) MANE Select	NP_001029288.1:p.Ala421Val
NM_001318965.2:c.1325C>T (EIF2B4)	NP_001305894.1:p.Ala442Val
NM_001318966.2:c.1217C>T (EIF2B4)	NP_001305895.1:p.Ala406Val
NM_001318967.2:c.1169C>T (EIF2B4)	NP_001305896.1:p.Ala390Val
NM_001318968.2:c.677C>T (EIF2B4)	NP_001305897.1:p.Ala226Val
NM_001318969.2:c.644C>T (EIF2B4)	NP_001305898.1:p.Ala215Val
NM_015636.4:c.1259C>T (EIF2B4)	NP_056451.3:p.Ala420Val
NM_172195.4:c.1322C>T (EIF2B4)	NP_751945.2:p.Ala441Val