Canonical Allele Identifier: CA355382281

Gene: EIF2B5

Linked Data

• dbSNP Id: rs1208399091
• gnomAD v2: 3-183855759-A-G
• gnomAD v4: 3-184137971-A-G
• MyVariant Identifiers: chr3:g.183855759A>G (hg19) ; chr3:g.184137971A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137971A>G , CM000665.2:g.184137971A>G	GRCh38
NC_000003.11:g.183855759A>G , CM000665.1:g.183855759A>G	GRCh37
NC_000003.10:g.185338453A>G	NCBI36
NG_015826.1:g.7950A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.603A>G
ENST00000468748.7:n.563A>G
ENST00000484154.2:n.1201A>G
ENST00000491008.6:n.1328A>G
ENST00000492226.2:n.577A>G
ENST00000492773.6:c.312A>G
ENST00000647636.1:c.580A>G	ENSP00000497505.1:p.Thr194Ala
ENST00000647909.1:c.604A>G	ENSP00000498164.1:p.Thr202Ala
ENST00000648145.1:c.348A>G
ENST00000648189.1:c.330A>G
ENST00000648256.1:c.529A>G	ENSP00000497356.1:p.Thr177Ala
ENST00000648314.1:c.580A>G	ENSP00000496920.1:p.Thr194Ala
ENST00000648599.1:c.580A>G	ENSP00000497159.1:p.Thr194Ala
ENST00000648630.1:c.574A>G	ENSP00000497887.1:p.Thr192Ala
ENST00000648682.1:c.580A>G	ENSP00000498185.1:p.Thr194Ala
ENST00000648882.1:c.*406A>G	ENSP00000497603.1:n.*406A>G
ENST00000648890.1:c.580A>G	ENSP00000497503.1:p.Thr194Ala
ENST00000648915.2:c.580A>G MANE Select	ENSP00000497160.1:p.Thr194Ala
ENST00000649545.1:c.314A>G
ENST00000649688.1:c.580A>G	ENSP00000497097.1:p.Thr194Ala
ENST00000649814.1:n.629A>G
ENST00000650270.1:c.447A>G
ENST00000273783.7:c.580A>G	ENSP00000273783.3:p.Thr194Ala
ENST00000432982.5:c.245+1296A>G
ENST00000444495.1:c.580A>G	ENSP00000409142.1:p.Thr194Ala
ENST00000468748.5:n.33A>G
ENST00000481054.5:n.581A>G
ENST00000491008.5:n.544A>G
ENST00000491144.5:n.1020A>G
ENST00000498831.1:n.535A>G
NM_003907.2:c.580A>G	NP_003898.2:p.Thr194Ala
XR_924208.1:n.1531A>G
NM_003907.3:c.580A>G MANE Select	NP_003898.2:p.Thr194Ala
XM_011513266.3:c.-322A>G	XP_011511568.1:n.-322A>G
XR_001740352.2:n.943A>G
XR_001740353.2:n.943A>G
XR_924208.2:n.943A>G