Canonical Allele Identifier: CA437323532

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855582T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137794T>G , CM000665.2:g.184137794T>G	GRCh38
NC_000003.11:g.183855582T>G , CM000665.1:g.183855582T>G	GRCh37
NC_000003.10:g.185338276T>G	NCBI36
NG_015826.1:g.7773T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.518T>G
ENST00000468748.7:n.478T>G
ENST00000484154.2:n.1116T>G
ENST00000491008.6:n.1243T>G
ENST00000492226.2:n.492T>G
ENST00000492773.6:c.227T>G
ENST00000647636.1:c.495T>G	ENSP00000497505.1:p.Leu165=
ENST00000647909.1:c.495T>G	ENSP00000498164.1:p.Leu165=
ENST00000648145.1:c.263T>G
ENST00000648189.1:c.245T>G
ENST00000648256.1:c.444T>G	ENSP00000497356.1:p.Leu148=
ENST00000648314.1:c.495T>G	ENSP00000496920.1:p.Leu165=
ENST00000648599.1:c.495T>G	ENSP00000497159.1:p.Leu165=
ENST00000648630.1:c.489T>G	ENSP00000497887.1:p.Leu163=
ENST00000648682.1:c.495T>G	ENSP00000498185.1:p.Leu165=
ENST00000648882.1:c.*321T>G	ENSP00000497603.1:n.*321T>G
ENST00000648890.1:c.495T>G	ENSP00000497503.1:p.Leu165=
ENST00000648915.2:c.495T>G MANE Select	ENSP00000497160.1:p.Leu165=
ENST00000649545.1:c.229T>G
ENST00000649688.1:c.495T>G	ENSP00000497097.1:p.Leu165=
ENST00000649814.1:n.544T>G
ENST00000650244.1:c.640T>G	ENSP00000497227.1:n.640T>G
ENST00000650270.1:c.362T>G
ENST00000273783.7:c.495T>G	ENSP00000273783.3:p.Leu165=
ENST00000432982.5:c.245+1119T>G
ENST00000444495.1:c.495T>G	ENSP00000409142.1:p.Leu165=
ENST00000481054.5:n.496T>G
ENST00000491008.5:n.459T>G
ENST00000491144.5:n.843T>G
ENST00000498831.1:n.450T>G
NM_003907.2:c.495T>G	NP_003898.2:p.Leu165=
XR_924208.1:n.1446T>G
NM_003907.3:c.495T>G MANE Select	NP_003898.2:p.Leu165=
XM_011513266.3:c.-407T>G	XP_011511568.1:n.-407T>G
XR_001740352.2:n.858T>G
XR_001740353.2:n.858T>G
XR_924208.2:n.858T>G