Canonical Allele Identifier: CA346197187

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587699T>C (hg19) ; chr2:g.27364832T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364832T>C , CM000664.2:g.27364832T>C	GRCh38
NC_000002.11:g.27587699T>C , CM000664.1:g.27587699T>C	GRCh37
NC_000002.10:g.27441203T>C	NCBI36
NG_009305.1:g.10626A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1258A>G (EIF2B4) MANE Select	ENSP00000233552.6:p.Thr420Ala
ENST00000347454.8:c.1258A>G (EIF2B4)	ENSP00000233552.5:p.Thr420Ala
ENST00000405940.6:c.*524A>G (EIF2B4)	ENSP00000384375.2:n.*524A>G
ENST00000445933.6:c.1255A>G (EIF2B4)	ENSP00000394397.2:p.Thr419Ala
ENST00000451130.6:c.1318A>G (EIF2B4)	ENSP00000394869.2:p.Thr440Ala
ENST00000478311.1:n.251A>G (EIF2B4)
ENST00000493344.6:c.1321A>G (EIF2B4)	ENSP00000429323.1:p.Thr441Ala
ENST00000616081.4:c.1249A>G (EIF2B4)	ENSP00000477710.1:p.Thr417Ala
ENST00000622434.4:c.*524A>G (EIF2B4)	ENSP00000479991.1:n.*524A>G
NM_001034116.1:c.1258A>G (EIF2B4)	NP_001029288.1:p.Thr420Ala
NM_015636.3:c.1255A>G (EIF2B4)	NP_056451.3:p.Thr419Ala
NM_172195.3:c.1318A>G (EIF2B4)	NP_751945.2:p.Thr440Ala
XM_005264632.1:c.1213A>G (EIF2B4)	XP_005264689.1:p.Thr405Ala
XM_006712132.1:c.1210A>G (EIF2B4)	XP_006712195.1:p.Thr404Ala
XM_011533147.1:c.640A>G (EIF2B4)	XP_011531449.1:p.Thr214Ala
XR_939868.1:n.1772-2592T>C (GTF3C2-AS2)
NM_001318965.1:c.1321A>G (EIF2B4)	NP_001305894.1:p.Thr441Ala
NM_001318966.1:c.1213A>G (EIF2B4)	NP_001305895.1:p.Thr405Ala
NM_001318967.1:c.1165A>G (EIF2B4)	NP_001305896.1:p.Thr389Ala
NM_001318968.1:c.673A>G (EIF2B4)	NP_001305897.1:p.Thr225Ala
NM_001318969.1:c.640A>G (EIF2B4)	NP_001305898.1:p.Thr214Ala
XM_011533147.2:c.640A>G (EIF2B4)	XP_011531449.1:p.Thr214Ala
NM_001034116.2:c.1258A>G (EIF2B4) MANE Select	NP_001029288.1:p.Thr420Ala
NM_001318965.2:c.1321A>G (EIF2B4)	NP_001305894.1:p.Thr441Ala
NM_001318966.2:c.1213A>G (EIF2B4)	NP_001305895.1:p.Thr405Ala
NM_001318967.2:c.1165A>G (EIF2B4)	NP_001305896.1:p.Thr389Ala
NM_001318968.2:c.673A>G (EIF2B4)	NP_001305897.1:p.Thr225Ala
NM_001318969.2:c.640A>G (EIF2B4)	NP_001305898.1:p.Thr214Ala
NM_015636.4:c.1255A>G (EIF2B4)	NP_056451.3:p.Thr419Ala
NM_172195.4:c.1318A>G (EIF2B4)	NP_751945.2:p.Thr440Ala