Canonical Allele Identifier: CA355381852

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855475T>A (hg19) ; chr3:g.184137687T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137687T>A , CM000665.2:g.184137687T>A	GRCh38
NC_000003.11:g.183855475T>A , CM000665.1:g.183855475T>A	GRCh37
NC_000003.10:g.185338169T>A	NCBI36
NG_015826.1:g.7666T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000465218.3:n.411T>A
ENST00000468748.7:n.371T>A
ENST00000484154.2:n.1009T>A
ENST00000491008.6:n.1136T>A
ENST00000492226.2:n.385T>A
ENST00000492773.6:c.120T>A
ENST00000647636.1:c.388T>A	ENSP00000497505.1:p.Ser130Thr
ENST00000647909.1:c.388T>A	ENSP00000498164.1:p.Ser130Thr
ENST00000648145.1:c.156T>A
ENST00000648189.1:c.138T>A
ENST00000648256.1:c.337T>A	ENSP00000497356.1:p.Ser113Thr
ENST00000648314.1:c.388T>A	ENSP00000496920.1:p.Ser130Thr
ENST00000648599.1:c.388T>A	ENSP00000497159.1:p.Ser130Thr
ENST00000648630.1:c.382T>A	ENSP00000497887.1:p.Ser128Thr
ENST00000648682.1:c.388T>A	ENSP00000498185.1:p.Ser130Thr
ENST00000648882.1:c.*214T>A	ENSP00000497603.1:n.*214T>A
ENST00000648890.1:c.388T>A	ENSP00000497503.1:p.Ser130Thr
ENST00000648915.2:c.388T>A MANE Select	ENSP00000497160.1:p.Ser130Thr
ENST00000649545.1:c.122T>A
ENST00000649688.1:c.388T>A	ENSP00000497097.1:p.Ser130Thr
ENST00000649814.1:n.437T>A
ENST00000650244.1:c.533T>A	ENSP00000497227.1:n.533T>A
ENST00000650270.1:c.255T>A
ENST00000273783.7:c.388T>A	ENSP00000273783.3:p.Ser130Thr
ENST00000432982.5:c.245+1012T>A
ENST00000444495.1:c.388T>A	ENSP00000409142.1:p.Ser130Thr
ENST00000481054.5:n.389T>A
ENST00000491008.5:n.352T>A
ENST00000491144.5:n.736T>A
ENST00000498831.1:n.343T>A
NM_003907.2:c.388T>A	NP_003898.2:p.Ser130Thr
XR_924208.1:n.1339T>A
NM_003907.3:c.388T>A MANE Select	NP_003898.2:p.Ser130Thr
XM_011513266.3:c.-514T>A	XP_011511568.1:n.-514T>A
XR_001740352.2:n.751T>A
XR_001740353.2:n.751T>A
XR_924208.2:n.751T>A