Canonical Allele Identifier: CA355382250

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184137957-C-A
• MyVariant Identifiers: chr3:g.183855745C>A (hg19) ; chr3:g.184137957C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137957C>A , CM000665.2:g.184137957C>A	GRCh38
NC_000003.11:g.183855745C>A , CM000665.1:g.183855745C>A	GRCh37
NC_000003.10:g.185338439C>A	NCBI36
NG_015826.1:g.7936C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.589C>A
ENST00000468748.7:n.549C>A
ENST00000484154.2:n.1187C>A
ENST00000491008.6:n.1314C>A
ENST00000492226.2:n.563C>A
ENST00000492773.6:c.298C>A
ENST00000647636.1:c.566C>A	ENSP00000497505.1:p.Ser189Tyr
ENST00000647909.1:c.590C>A	ENSP00000498164.1:p.Ser197Tyr
ENST00000648145.1:c.334C>A
ENST00000648189.1:c.316C>A
ENST00000648256.1:c.515C>A	ENSP00000497356.1:p.Ser172Tyr
ENST00000648314.1:c.566C>A	ENSP00000496920.1:p.Ser189Tyr
ENST00000648599.1:c.566C>A	ENSP00000497159.1:p.Ser189Tyr
ENST00000648630.1:c.560C>A	ENSP00000497887.1:p.Ser187Tyr
ENST00000648682.1:c.566C>A	ENSP00000498185.1:p.Ser189Tyr
ENST00000648882.1:c.*392C>A	ENSP00000497603.1:n.*392C>A
ENST00000648890.1:c.566C>A	ENSP00000497503.1:p.Ser189Tyr
ENST00000648915.2:c.566C>A MANE Select	ENSP00000497160.1:p.Ser189Tyr
ENST00000649545.1:c.300C>A
ENST00000649688.1:c.566C>A	ENSP00000497097.1:p.Ser189Tyr
ENST00000649814.1:n.615C>A
ENST00000650270.1:c.433C>A
ENST00000273783.7:c.566C>A	ENSP00000273783.3:p.Ser189Tyr
ENST00000432982.5:c.245+1282C>A
ENST00000444495.1:c.566C>A	ENSP00000409142.1:p.Ser189Tyr
ENST00000468748.5:n.19C>A
ENST00000481054.5:n.567C>A
ENST00000491008.5:n.530C>A
ENST00000491144.5:n.1006C>A
ENST00000498831.1:n.521C>A
NM_003907.2:c.566C>A	NP_003898.2:p.Ser189Tyr
XR_924208.1:n.1517C>A
NM_003907.3:c.566C>A MANE Select	NP_003898.2:p.Ser189Tyr
XM_011513266.3:c.-336C>A	XP_011511568.1:n.-336C>A
XR_001740352.2:n.929C>A
XR_001740353.2:n.929C>A
XR_924208.2:n.929C>A