Canonical Allele Identifier: CA355382367

Gene: EIF2B5

Linked Data

• dbSNP Id: rs1307137552
• gnomAD v2: 3-183855801-A-G
• gnomAD v3: 3-184138013-A-G
• gnomAD v4: 3-184138013-A-G
• MyVariant Identifiers: chr3:g.183855801A>G (hg19) ; chr3:g.184138013A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138013A>G , CM000665.2:g.184138013A>G	GRCh38
NC_000003.11:g.183855801A>G , CM000665.1:g.183855801A>G	GRCh37
NC_000003.10:g.185338495A>G	NCBI36
NG_015826.1:g.7992A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.645A>G
ENST00000468748.7:n.605A>G
ENST00000484154.2:n.1243A>G
ENST00000491008.6:n.1370A>G
ENST00000492226.2:n.619A>G
ENST00000492773.6:c.354A>G
ENST00000647636.1:c.622A>G	ENSP00000497505.1:p.Thr208Ala
ENST00000647909.1:c.646A>G	ENSP00000498164.1:p.Thr216Ala
ENST00000648145.1:c.390A>G
ENST00000648189.1:c.372A>G
ENST00000648256.1:c.571A>G	ENSP00000497356.1:p.Thr191Ala
ENST00000648314.1:c.622A>G	ENSP00000496920.1:p.Thr208Ala
ENST00000648599.1:c.622A>G	ENSP00000497159.1:p.Thr208Ala
ENST00000648630.1:c.616A>G	ENSP00000497887.1:p.Thr206Ala
ENST00000648682.1:c.622A>G	ENSP00000498185.1:p.Thr208Ala
ENST00000648882.1:c.*448A>G	ENSP00000497603.1:n.*448A>G
ENST00000648890.1:c.622A>G	ENSP00000497503.1:p.Thr208Ala
ENST00000648915.2:c.622A>G MANE Select	ENSP00000497160.1:p.Thr208Ala
ENST00000649545.1:c.356A>G
ENST00000649688.1:c.622A>G	ENSP00000497097.1:p.Thr208Ala
ENST00000649814.1:n.671A>G
ENST00000650270.1:c.489A>G
ENST00000273783.7:c.622A>G	ENSP00000273783.3:p.Thr208Ala
ENST00000432982.5:c.245+1338A>G
ENST00000444495.1:c.622A>G	ENSP00000409142.1:p.Thr208Ala
ENST00000468748.5:n.75A>G
ENST00000481054.5:n.623A>G
ENST00000491008.5:n.586A>G
ENST00000491144.5:n.1062A>G
ENST00000498831.1:n.577A>G
NM_003907.2:c.622A>G	NP_003898.2:p.Thr208Ala
XR_924208.1:n.1573A>G
NM_003907.3:c.622A>G MANE Select	NP_003898.2:p.Thr208Ala
XM_011513266.3:c.-280A>G	XP_011511568.1:n.-280A>G
XR_001740352.2:n.985A>G
XR_001740353.2:n.985A>G
XR_924208.2:n.985A>G