Canonical Allele Identifier: CA355382936

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855982T>G (hg19) ; chr3:g.184138194T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138194T>G , CM000665.2:g.184138194T>G	GRCh38
NC_000003.11:g.183855982T>G , CM000665.1:g.183855982T>G	GRCh37
NC_000003.10:g.185338676T>G	NCBI36
NG_015826.1:g.8173T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.736T>G
ENST00000468748.7:n.696T>G
ENST00000484154.2:n.1334T>G
ENST00000491008.6:n.1461T>G
ENST00000492226.2:n.710T>G
ENST00000492773.6:c.467T>G
ENST00000647636.1:c.713T>G	ENSP00000497505.1:p.Val238Gly
ENST00000647909.1:c.737T>G	ENSP00000498164.1:p.Val246Gly
ENST00000648145.1:c.481T>G
ENST00000648189.1:c.463T>G
ENST00000648256.1:c.662T>G	ENSP00000497356.1:p.Val221Gly
ENST00000648314.1:c.713T>G	ENSP00000496920.1:p.Val238Gly
ENST00000648599.1:c.713T>G	ENSP00000497159.1:p.Val238Gly
ENST00000648630.1:c.707T>G	ENSP00000497887.1:p.Val236Gly
ENST00000648682.1:c.713T>G	ENSP00000498185.1:p.Val238Gly
ENST00000648882.1:c.*539T>G	ENSP00000497603.1:n.*539T>G
ENST00000648890.1:c.713T>G	ENSP00000497503.1:p.Val238Gly
ENST00000648915.2:c.713T>G MANE Select	ENSP00000497160.1:p.Val238Gly
ENST00000649545.1:c.447T>G
ENST00000649688.1:c.713T>G	ENSP00000497097.1:p.Val238Gly
ENST00000649814.1:n.762T>G
ENST00000650270.1:c.580T>G
ENST00000273783.7:c.713T>G	ENSP00000273783.3:p.Val238Gly
ENST00000432982.5:c.245+1519T>G
ENST00000444495.1:c.713T>G	ENSP00000409142.1:p.Val238Gly
ENST00000468748.5:n.166T>G
ENST00000479833.1:n.29T>G
ENST00000481054.5:n.714T>G
ENST00000491008.5:n.677T>G
ENST00000491144.5:n.1153T>G
NM_003907.2:c.713T>G	NP_003898.2:p.Val238Gly
XR_924208.1:n.1664T>G
NM_003907.3:c.713T>G MANE Select	NP_003898.2:p.Val238Gly
XM_011513266.3:c.-189T>G	XP_011511568.1:n.-189T>G
XR_001740352.2:n.1076T>G
XR_001740353.2:n.1076T>G
XR_924208.2:n.1076T>G