Canonical Allele Identifier: CA2668795881

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184136952-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136952C>G , CM000665.2:g.184136952C>G	GRCh38
NC_000003.11:g.183854740C>G , CM000665.1:g.183854740C>G	GRCh37
NC_000003.10:g.185337434C>G	NCBI36
NG_015826.1:g.6931C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.*212C>G	ENSP00000414775.1:n.*212C>G
ENST00000465218.3:n.343+216C>G
ENST00000468748.7:n.303+216C>G
ENST00000471832.2:c.*530C>G	ENSP00000497786.1:n.*530C>G
ENST00000484154.2:n.274C>G
ENST00000491008.6:n.401C>G
ENST00000492226.2:n.317+216C>G
ENST00000492773.6:c.52+216C>G
ENST00000647636.1:c.320+216C>G	ENSP00000497505.1:n.320+216C>G
ENST00000647909.1:c.320+216C>G	ENSP00000498164.1:n.320+216C>G
ENST00000648145.1:c.88+216C>G
ENST00000648189.1:c.70+216C>G
ENST00000648256.1:c.269+216C>G	ENSP00000497356.1:n.269+216C>G
ENST00000648314.1:c.320+216C>G	ENSP00000496920.1:n.320+216C>G
ENST00000648599.1:c.320+216C>G	ENSP00000497159.1:n.320+216C>G
ENST00000648630.1:c.314+216C>G	ENSP00000497887.1:n.314+216C>G
ENST00000648682.1:c.320+216C>G	ENSP00000498185.1:n.320+216C>G
ENST00000648882.1:c.*146+216C>G	ENSP00000497603.1:n.*146+216C>G
ENST00000648890.1:c.320+216C>G	ENSP00000497503.1:n.320+216C>G
ENST00000648915.2:c.320+216C>G MANE Select	ENSP00000497160.1:n.320+216C>G
ENST00000649545.1:c.54+216C>G
ENST00000649688.1:c.320+216C>G	ENSP00000497097.1:n.320+216C>G
ENST00000649814.1:n.369+216C>G
ENST00000650244.1:c.465+216C>G	ENSP00000497227.1:n.465+216C>G
ENST00000650270.1:c.187+216C>G
ENST00000273783.7:c.320+216C>G	ENSP00000273783.3:n.320+216C>G
ENST00000432569.1:c.*212C>G	ENSP00000414775.1:n.*212C>G
ENST00000432982.5:c.245+277C>G
ENST00000444495.1:c.320+216C>G	ENSP00000409142.1:n.320+216C>G
ENST00000471832.1:n.467C>G
ENST00000481054.5:n.321+216C>G
ENST00000491144.5:n.668+216C>G
ENST00000498831.1:n.176+216C>G
NM_003907.2:c.320+216C>G	NP_003898.2:n.320+216C>G
XR_924208.1:n.1271+216C>G
NM_003907.3:c.320+216C>G MANE Select	NP_003898.2:n.320+216C>G
XM_011513266.3:c.-582+216C>G	XP_011511568.1:n.-582+216C>G
XR_001740352.2:n.683+216C>G
XR_001740353.2:n.683+216C>G
XR_924208.2:n.683+216C>G