Canonical Allele Identifier: CA2668796229

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184137608-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137608C>A , CM000665.2:g.184137608C>A	GRCh38
NC_000003.11:g.183855396C>A , CM000665.1:g.183855396C>A	GRCh37
NC_000003.10:g.185338090C>A	NCBI36
NG_015826.1:g.7587C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000465218.3:n.344-12C>A
ENST00000468748.7:n.304-12C>A
ENST00000484154.2:n.930C>A
ENST00000491008.6:n.1057C>A
ENST00000492226.2:n.318-12C>A
ENST00000492773.6:c.53-12C>A
ENST00000647636.1:c.321-12C>A	ENSP00000497505.1:n.321-12C>A
ENST00000647909.1:c.321-12C>A	ENSP00000498164.1:n.321-12C>A
ENST00000648145.1:c.89-12C>A
ENST00000648189.1:c.71-12C>A
ENST00000648256.1:c.270-12C>A	ENSP00000497356.1:n.270-12C>A
ENST00000648314.1:c.321-12C>A	ENSP00000496920.1:n.321-12C>A
ENST00000648599.1:c.321-12C>A	ENSP00000497159.1:n.321-12C>A
ENST00000648630.1:c.315-12C>A	ENSP00000497887.1:n.315-12C>A
ENST00000648682.1:c.321-12C>A	ENSP00000498185.1:n.321-12C>A
ENST00000648882.1:c.*147-12C>A	ENSP00000497603.1:n.*147-12C>A
ENST00000648890.1:c.321-12C>A	ENSP00000497503.1:n.321-12C>A
ENST00000648915.2:c.321-12C>A MANE Select	ENSP00000497160.1:n.321-12C>A
ENST00000649545.1:c.55-12C>A
ENST00000649688.1:c.321-12C>A	ENSP00000497097.1:n.321-12C>A
ENST00000649814.1:n.370-12C>A
ENST00000650244.1:c.466-12C>A	ENSP00000497227.1:n.466-12C>A
ENST00000650270.1:c.188-12C>A
ENST00000273783.7:c.321-12C>A	ENSP00000273783.3:n.321-12C>A
ENST00000432982.5:c.245+933C>A
ENST00000444495.1:c.321-12C>A	ENSP00000409142.1:n.321-12C>A
ENST00000481054.5:n.322-12C>A
ENST00000491008.5:n.273C>A
ENST00000491144.5:n.669-12C>A
ENST00000498831.1:n.276-12C>A
NM_003907.2:c.321-12C>A	NP_003898.2:n.321-12C>A
XR_924208.1:n.1272-12C>A
NM_003907.3:c.321-12C>A MANE Select	NP_003898.2:n.321-12C>A
XM_011513266.3:c.-581-12C>A	XP_011511568.1:n.-581-12C>A
XR_001740352.2:n.684-12C>A
XR_001740353.2:n.684-12C>A
XR_924208.2:n.684-12C>A