Canonical Allele Identifier: CA346197263

Gene: EIF2B4 GTF3C2-AS2

Linked Data

• MyVariant Identifiers: chr2:g.27587726T>A (hg19) ; chr2:g.27364859T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27364859T>A , CM000664.2:g.27364859T>A	GRCh38
NC_000002.11:g.27587726T>A , CM000664.1:g.27587726T>A	GRCh37
NC_000002.10:g.27441230T>A	NCBI36
NG_009305.1:g.10599A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.1231A>T (EIF2B4) MANE Select	ENSP00000233552.6:p.Asn411Tyr
ENST00000347454.8:c.1231A>T (EIF2B4)	ENSP00000233552.5:p.Asn411Tyr
ENST00000405940.6:c.*497A>T (EIF2B4)	ENSP00000384375.2:n.*497A>T
ENST00000445933.6:c.1228A>T (EIF2B4)	ENSP00000394397.2:p.Asn410Tyr
ENST00000451130.6:c.1291A>T (EIF2B4)	ENSP00000394869.2:p.Asn431Tyr
ENST00000478311.1:n.224A>T (EIF2B4)
ENST00000493344.6:c.1294A>T (EIF2B4)	ENSP00000429323.1:p.Asn432Tyr
ENST00000616081.4:c.1222A>T (EIF2B4)	ENSP00000477710.1:p.Asn408Tyr
ENST00000622434.4:c.*497A>T (EIF2B4)	ENSP00000479991.1:n.*497A>T
NM_001034116.1:c.1231A>T (EIF2B4)	NP_001029288.1:p.Asn411Tyr
NM_015636.3:c.1228A>T (EIF2B4)	NP_056451.3:p.Asn410Tyr
NM_172195.3:c.1291A>T (EIF2B4)	NP_751945.2:p.Asn431Tyr
XM_005264632.1:c.1186A>T (EIF2B4)	XP_005264689.1:p.Asn396Tyr
XM_006712132.1:c.1183A>T (EIF2B4)	XP_006712195.1:p.Asn395Tyr
XM_011533147.1:c.613A>T (EIF2B4)	XP_011531449.1:p.Asn205Tyr
XR_939868.1:n.1772-2565T>A (GTF3C2-AS2)
NM_001318965.1:c.1294A>T (EIF2B4)	NP_001305894.1:p.Asn432Tyr
NM_001318966.1:c.1186A>T (EIF2B4)	NP_001305895.1:p.Asn396Tyr
NM_001318967.1:c.1138A>T (EIF2B4)	NP_001305896.1:p.Asn380Tyr
NM_001318968.1:c.646A>T (EIF2B4)	NP_001305897.1:p.Asn216Tyr
NM_001318969.1:c.613A>T (EIF2B4)	NP_001305898.1:p.Asn205Tyr
XM_011533147.2:c.613A>T (EIF2B4)	XP_011531449.1:p.Asn205Tyr
NM_001034116.2:c.1231A>T (EIF2B4) MANE Select	NP_001029288.1:p.Asn411Tyr
NM_001318965.2:c.1294A>T (EIF2B4)	NP_001305894.1:p.Asn432Tyr
NM_001318966.2:c.1186A>T (EIF2B4)	NP_001305895.1:p.Asn396Tyr
NM_001318967.2:c.1138A>T (EIF2B4)	NP_001305896.1:p.Asn380Tyr
NM_001318968.2:c.646A>T (EIF2B4)	NP_001305897.1:p.Asn216Tyr
NM_001318969.2:c.613A>T (EIF2B4)	NP_001305898.1:p.Asn205Tyr
NM_015636.4:c.1228A>T (EIF2B4)	NP_056451.3:p.Asn410Tyr
NM_172195.4:c.1291A>T (EIF2B4)	NP_751945.2:p.Asn431Tyr