Canonical Allele Identifier: CA1240245878

Gene: EIF2B4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27367844C= , CM000664.2:g.27367844C=	GRCh38
NC_000002.11:g.27590711C= , CM000664.1:g.27590711C=	GRCh37
NC_000002.10:g.27444215C=	NCBI36
NG_009305.1:g.7614G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347454.9:c.706-22G= MANE Select	ENSP00000233552.6:n.706-22G=
ENST00000347454.8:c.706-22G=	ENSP00000233552.5:n.706-22G=
ENST00000405940.6:c.680-22G=	ENSP00000384375.2:n.680-22G=
ENST00000417567.1:c.282-22G=
ENST00000445933.6:c.703-22G=	ENSP00000394397.2:n.703-22G=
ENST00000451130.6:c.766-22G=	ENSP00000394869.2:n.766-22G=
ENST00000475582.5:n.2007G=
ENST00000493344.6:c.769-22G=	ENSP00000429323.1:n.769-22G=
ENST00000616081.4:c.697-22G=	ENSP00000477710.1:n.697-22G=
ENST00000622434.4:c.661-22G=	ENSP00000479991.1:n.661-22G=
NM_001034116.1:c.706-22G=	NP_001029288.1:n.706-22G=
NM_015636.3:c.703-22G=	NP_056451.3:n.703-22G=
NM_172195.3:c.766-22G=	NP_751945.2:n.766-22G=
XM_005264632.1:c.661-22G=	XP_005264689.1:n.661-22G=
XM_006712132.1:c.658-22G=	XP_006712195.1:n.658-22G=
XM_011533147.1:c.88-22G=	XP_011531449.1:n.88-22G=
NM_001318965.1:c.769-22G=	NP_001305894.1:n.769-22G=
NM_001318966.1:c.661-22G=	NP_001305895.1:n.661-22G=
NM_001318967.1:c.613-22G=	NP_001305896.1:n.613-22G=
NM_001318968.1:c.121-22G=	NP_001305897.1:n.121-22G=
NM_001318969.1:c.88-22G=	NP_001305898.1:n.88-22G=
XM_011533147.2:c.88-22G=	XP_011531449.1:n.88-22G=
NM_001034116.2:c.706-22G= MANE Select	NP_001029288.1:n.706-22G=
NM_001318965.2:c.769-22G=	NP_001305894.1:n.769-22G=
NM_001318966.2:c.661-22G=	NP_001305895.1:n.661-22G=
NM_001318967.2:c.613-22G=	NP_001305896.1:n.613-22G=
NM_001318968.2:c.121-22G=	NP_001305897.1:n.121-22G=
NM_001318969.2:c.88-22G=	NP_001305898.1:n.88-22G=
NM_015636.4:c.703-22G=	NP_056451.3:n.703-22G=
NM_172195.4:c.766-22G=	NP_751945.2:n.766-22G=