Canonical Allele Identifier: CA355382468

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855850T>A (hg19) ; chr3:g.184138062T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138062T>A , CM000665.2:g.184138062T>A	GRCh38
NC_000003.11:g.183855850T>A , CM000665.1:g.183855850T>A	GRCh37
NC_000003.10:g.185338544T>A	NCBI36
NG_015826.1:g.8041T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.694T>A
ENST00000468748.7:n.654T>A
ENST00000484154.2:n.1292T>A
ENST00000491008.6:n.1419T>A
ENST00000492226.2:n.668T>A
ENST00000492773.6:c.403T>A
ENST00000647636.1:c.671T>A	ENSP00000497505.1:p.Phe224Tyr
ENST00000647909.1:c.695T>A	ENSP00000498164.1:p.Phe232Tyr
ENST00000648145.1:c.439T>A
ENST00000648189.1:c.421T>A
ENST00000648256.1:c.620T>A	ENSP00000497356.1:p.Phe207Tyr
ENST00000648314.1:c.671T>A	ENSP00000496920.1:p.Phe224Tyr
ENST00000648599.1:c.671T>A	ENSP00000497159.1:p.Phe224Tyr
ENST00000648630.1:c.665T>A	ENSP00000497887.1:p.Phe222Tyr
ENST00000648682.1:c.671T>A	ENSP00000498185.1:p.Phe224Tyr
ENST00000648882.1:c.*497T>A	ENSP00000497603.1:n.*497T>A
ENST00000648890.1:c.671T>A	ENSP00000497503.1:p.Phe224Tyr
ENST00000648915.2:c.671T>A MANE Select	ENSP00000497160.1:p.Phe224Tyr
ENST00000649545.1:c.405T>A
ENST00000649688.1:c.671T>A	ENSP00000497097.1:p.Phe224Tyr
ENST00000649814.1:n.720T>A
ENST00000650270.1:c.538T>A
ENST00000273783.7:c.671T>A	ENSP00000273783.3:p.Phe224Tyr
ENST00000432982.5:c.245+1387T>A
ENST00000444495.1:c.671T>A	ENSP00000409142.1:p.Phe224Tyr
ENST00000468748.5:n.124T>A
ENST00000481054.5:n.672T>A
ENST00000491008.5:n.635T>A
ENST00000491144.5:n.1111T>A
NM_003907.2:c.671T>A	NP_003898.2:p.Phe224Tyr
XR_924208.1:n.1622T>A
NM_003907.3:c.671T>A MANE Select	NP_003898.2:p.Phe224Tyr
XM_011513266.3:c.-231T>A	XP_011511568.1:n.-231T>A
XR_001740352.2:n.1034T>A
XR_001740353.2:n.1034T>A
XR_924208.2:n.1034T>A