Canonical Allele Identifier: CA2697557006

Gene: EIF2B5

Linked Data

• ClinVar Variation Id: 2763481
• ClinVar RCV Id: RCV003565110

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138092G>A , CM000665.2:g.184138092G>A	GRCh38
NC_000003.11:g.183855880G>A , CM000665.1:g.183855880G>A	GRCh37
NC_000003.10:g.185338574G>A	NCBI36
NG_015826.1:g.8071G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.707+17G>A
ENST00000468748.7:n.667+17G>A
ENST00000484154.2:n.1305+17G>A
ENST00000491008.6:n.1432+17G>A
ENST00000492226.2:n.681+17G>A
ENST00000492773.6:c.416+17G>A
ENST00000647636.1:c.684+17G>A	ENSP00000497505.1:n.684+17G>A
ENST00000647909.1:c.708+17G>A	ENSP00000498164.1:n.708+17G>A
ENST00000648145.1:c.452+17G>A
ENST00000648189.1:c.434+17G>A
ENST00000648256.1:c.633+17G>A	ENSP00000497356.1:n.633+17G>A
ENST00000648314.1:c.684+17G>A	ENSP00000496920.1:n.684+17G>A
ENST00000648599.1:c.684+17G>A	ENSP00000497159.1:n.684+17G>A
ENST00000648630.1:c.678+17G>A	ENSP00000497887.1:n.678+17G>A
ENST00000648682.1:c.684+17G>A	ENSP00000498185.1:n.684+17G>A
ENST00000648882.1:c.*510+17G>A	ENSP00000497603.1:n.*510+17G>A
ENST00000648890.1:c.684+17G>A	ENSP00000497503.1:n.684+17G>A
ENST00000648915.2:c.684+17G>A MANE Select	ENSP00000497160.1:n.684+17G>A
ENST00000649545.1:c.418+17G>A
ENST00000649688.1:c.684+17G>A	ENSP00000497097.1:n.684+17G>A
ENST00000649814.1:n.733+17G>A
ENST00000650270.1:c.551+17G>A
ENST00000273783.7:c.684+17G>A	ENSP00000273783.3:n.684+17G>A
ENST00000432982.5:c.245+1417G>A
ENST00000444495.1:c.684+17G>A	ENSP00000409142.1:n.684+17G>A
ENST00000468748.5:n.137+17G>A
ENST00000481054.5:n.685+17G>A
ENST00000491008.5:n.648+17G>A
ENST00000491144.5:n.1124+17G>A
NM_003907.2:c.684+17G>A	NP_003898.2:n.684+17G>A
XR_924208.1:n.1635+17G>A
NM_003907.3:c.684+17G>A MANE Select	NP_003898.2:n.684+17G>A
XM_011513266.3:c.-218+17G>A	XP_011511568.1:n.-218+17G>A
XR_001740352.2:n.1047+17G>A
XR_001740353.2:n.1047+17G>A
XR_924208.2:n.1047+17G>A