Canonical Allele Identifier: CA355382887

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855971T>A (hg19) ; chr3:g.184138183T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138183T>A , CM000665.2:g.184138183T>A	GRCh38
NC_000003.11:g.183855971T>A , CM000665.1:g.183855971T>A	GRCh37
NC_000003.10:g.185338665T>A	NCBI36
NG_015826.1:g.8162T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.725T>A
ENST00000468748.7:n.685T>A
ENST00000484154.2:n.1323T>A
ENST00000491008.6:n.1450T>A
ENST00000492226.2:n.699T>A
ENST00000492773.6:c.456T>A
ENST00000647636.1:c.702T>A	ENSP00000497505.1:p.Ser234Arg
ENST00000647909.1:c.726T>A	ENSP00000498164.1:p.Ser242Arg
ENST00000648145.1:c.470T>A
ENST00000648189.1:c.452T>A
ENST00000648256.1:c.651T>A	ENSP00000497356.1:p.Ser217Arg
ENST00000648314.1:c.702T>A	ENSP00000496920.1:p.Ser234Arg
ENST00000648599.1:c.702T>A	ENSP00000497159.1:p.Ser234Arg
ENST00000648630.1:c.696T>A	ENSP00000497887.1:p.Ser232Arg
ENST00000648682.1:c.702T>A	ENSP00000498185.1:p.Ser234Arg
ENST00000648882.1:c.*528T>A	ENSP00000497603.1:n.*528T>A
ENST00000648890.1:c.702T>A	ENSP00000497503.1:p.Ser234Arg
ENST00000648915.2:c.702T>A MANE Select	ENSP00000497160.1:p.Ser234Arg
ENST00000649545.1:c.436T>A
ENST00000649688.1:c.702T>A	ENSP00000497097.1:p.Ser234Arg
ENST00000649814.1:n.751T>A
ENST00000650270.1:c.569T>A
ENST00000273783.7:c.702T>A	ENSP00000273783.3:p.Ser234Arg
ENST00000432982.5:c.245+1508T>A
ENST00000444495.1:c.702T>A	ENSP00000409142.1:p.Ser234Arg
ENST00000468748.5:n.155T>A
ENST00000479833.1:n.18T>A
ENST00000481054.5:n.703T>A
ENST00000491008.5:n.666T>A
ENST00000491144.5:n.1142T>A
NM_003907.2:c.702T>A	NP_003898.2:p.Ser234Arg
XR_924208.1:n.1653T>A
NM_003907.3:c.702T>A MANE Select	NP_003898.2:p.Ser234Arg
XM_011513266.3:c.-200T>A	XP_011511568.1:n.-200T>A
XR_001740352.2:n.1065T>A
XR_001740353.2:n.1065T>A
XR_924208.2:n.1065T>A