Canonical Allele Identifier: CA355382241

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855741T>A (hg19) ; chr3:g.184137953T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137953T>A , CM000665.2:g.184137953T>A	GRCh38
NC_000003.11:g.183855741T>A , CM000665.1:g.183855741T>A	GRCh37
NC_000003.10:g.185338435T>A	NCBI36
NG_015826.1:g.7932T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.585T>A
ENST00000468748.7:n.545T>A
ENST00000484154.2:n.1183T>A
ENST00000491008.6:n.1310T>A
ENST00000492226.2:n.559T>A
ENST00000492773.6:c.294T>A
ENST00000647636.1:c.562T>A	ENSP00000497505.1:p.Ser188Thr
ENST00000647909.1:c.586T>A	ENSP00000498164.1:p.Ser196Thr
ENST00000648145.1:c.330T>A
ENST00000648189.1:c.312T>A
ENST00000648256.1:c.511T>A	ENSP00000497356.1:p.Ser171Thr
ENST00000648314.1:c.562T>A	ENSP00000496920.1:p.Ser188Thr
ENST00000648599.1:c.562T>A	ENSP00000497159.1:p.Ser188Thr
ENST00000648630.1:c.556T>A	ENSP00000497887.1:p.Ser186Thr
ENST00000648682.1:c.562T>A	ENSP00000498185.1:p.Ser188Thr
ENST00000648882.1:c.*388T>A	ENSP00000497603.1:n.*388T>A
ENST00000648890.1:c.562T>A	ENSP00000497503.1:p.Ser188Thr
ENST00000648915.2:c.562T>A MANE Select	ENSP00000497160.1:p.Ser188Thr
ENST00000649545.1:c.296T>A
ENST00000649688.1:c.562T>A	ENSP00000497097.1:p.Ser188Thr
ENST00000649814.1:n.611T>A
ENST00000650270.1:c.429T>A
ENST00000273783.7:c.562T>A	ENSP00000273783.3:p.Ser188Thr
ENST00000432982.5:c.245+1278T>A
ENST00000444495.1:c.562T>A	ENSP00000409142.1:p.Ser188Thr
ENST00000468748.5:n.15T>A
ENST00000481054.5:n.563T>A
ENST00000491008.5:n.526T>A
ENST00000491144.5:n.1002T>A
ENST00000498831.1:n.517T>A
NM_003907.2:c.562T>A	NP_003898.2:p.Ser188Thr
XR_924208.1:n.1513T>A
NM_003907.3:c.562T>A MANE Select	NP_003898.2:p.Ser188Thr
XM_011513266.3:c.-340T>A	XP_011511568.1:n.-340T>A
XR_001740352.2:n.925T>A
XR_001740353.2:n.925T>A
XR_924208.2:n.925T>A