Canonical Allele Identifier: CA1425885459

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184140347A= , CM000665.2:g.184140347A=	GRCh38
NC_000003.11:g.183858135A= , CM000665.1:g.183858135A=	GRCh37
NC_000003.10:g.185340829A=	NCBI36
NG_015826.1:g.10326A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.867-71A=
ENST00000468748.7:n.1016A=
ENST00000484154.2:n.1387-1578A=
ENST00000491008.6:n.1592-71A=
ENST00000492226.2:n.1030A=
ENST00000492773.6:c.598-71A=
ENST00000647636.1:c.844-71A=	ENSP00000497505.1:n.844-71A=
ENST00000647909.1:c.868-71A=	ENSP00000498164.1:n.868-71A=
ENST00000648145.1:c.612-71A=
ENST00000648189.1:c.658-71A=
ENST00000648256.1:c.816-71A=	ENSP00000497356.1:n.816-71A=
ENST00000648314.1:c.908-71A=	ENSP00000496920.1:n.908-71A=
ENST00000648599.1:c.*127-71A=	ENSP00000497159.1:n.*127-71A=
ENST00000648630.1:c.838-71A=	ENSP00000497887.1:n.838-71A=
ENST00000648682.1:c.844-71A=	ENSP00000498185.1:n.844-71A=
ENST00000648882.1:c.*670-71A=	ENSP00000497603.1:n.*670-71A=
ENST00000648890.1:c.844-71A=	ENSP00000497503.1:n.844-71A=
ENST00000648915.2:c.844-71A= MANE Select	ENSP00000497160.1:n.844-71A=
ENST00000649545.1:c.577+190A=
ENST00000649688.1:c.*127-71A=	ENSP00000497097.1:n.*127-71A=
ENST00000649814.1:n.893-71A=
ENST00000650270.1:c.711-71A=
ENST00000273783.7:c.844-71A=	ENSP00000273783.3:n.844-71A=
ENST00000432982.5:c.246-1890A=
ENST00000444495.1:c.844-71A=	ENSP00000409142.1:n.844-71A=
ENST00000468748.5:n.486A=
ENST00000479833.1:n.160-71A=
ENST00000481054.5:n.938-71A=
ENST00000491144.5:n.1348-71A=
ENST00000493740.1:n.74-71A=
NM_003907.2:c.844-71A=	NP_003898.2:n.844-71A=
XM_011513265.1:c.94-71A=	XP_011511567.1:n.94-71A=
XM_011513266.1:c.7-71A=	XP_011511568.1:n.7-71A=
XR_924208.1:n.1795-71A=
NM_003907.3:c.844-71A= MANE Select	NP_003898.2:n.844-71A=
XM_011513266.3:c.7-71A=	XP_011511568.1:n.7-71A=
XR_001740352.2:n.1207-71A=
XR_001740353.2:n.1207-71A=
XR_924208.2:n.1207-71A=