Canonical Allele Identifier: CA1240246014

Gene: EIF2B4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27367977T= , CM000664.2:g.27367977T=	GRCh38
NC_000002.11:g.27590844T= , CM000664.1:g.27590844T=	GRCh37
NC_000002.10:g.27444348T=	NCBI36
NG_009305.1:g.7481A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000347454.9:c.705+48A= MANE Select	ENSP00000233552.6:n.705+48A=
ENST00000347454.8:c.705+48A=	ENSP00000233552.5:n.705+48A=
ENST00000405940.6:c.679+48A=	ENSP00000384375.2:n.679+48A=
ENST00000417567.1:c.281+48A=
ENST00000445933.6:c.702+48A=	ENSP00000394397.2:n.702+48A=
ENST00000451130.6:c.765+48A=	ENSP00000394869.2:n.765+48A=
ENST00000475582.5:n.1874A=
ENST00000493344.6:c.768+48A=	ENSP00000429323.1:n.768+48A=
ENST00000616081.4:c.696+48A=	ENSP00000477710.1:n.696+48A=
ENST00000622434.4:c.660+48A=	ENSP00000479991.1:n.660+48A=
NM_001034116.1:c.705+48A=	NP_001029288.1:n.705+48A=
NM_015636.3:c.702+48A=	NP_056451.3:n.702+48A=
NM_172195.3:c.765+48A=	NP_751945.2:n.765+48A=
XM_005264632.1:c.660+48A=	XP_005264689.1:n.660+48A=
XM_006712132.1:c.657+48A=	XP_006712195.1:n.657+48A=
XM_011533147.1:c.87+48A=	XP_011531449.1:n.87+48A=
NM_001318965.1:c.768+48A=	NP_001305894.1:n.768+48A=
NM_001318966.1:c.660+48A=	NP_001305895.1:n.660+48A=
NM_001318967.1:c.612+48A=	NP_001305896.1:n.612+48A=
NM_001318968.1:c.120+48A=	NP_001305897.1:n.120+48A=
NM_001318969.1:c.87+48A=	NP_001305898.1:n.87+48A=
XM_011533147.2:c.87+48A=	XP_011531449.1:n.87+48A=
NM_001034116.2:c.705+48A= MANE Select	NP_001029288.1:n.705+48A=
NM_001318965.2:c.768+48A=	NP_001305894.1:n.768+48A=
NM_001318966.2:c.660+48A=	NP_001305895.1:n.660+48A=
NM_001318967.2:c.612+48A=	NP_001305896.1:n.612+48A=
NM_001318968.2:c.120+48A=	NP_001305897.1:n.120+48A=
NM_001318969.2:c.87+48A=	NP_001305898.1:n.87+48A=
NM_015636.4:c.702+48A=	NP_056451.3:n.702+48A=
NM_172195.4:c.765+48A=	NP_751945.2:n.765+48A=