Canonical Allele Identifier: CA2726569

Gene: EIF2B5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184140589C>T , CM000665.2:g.184140589C>T	GRCh38
NC_000003.11:g.183858377C>T , CM000665.1:g.183858377C>T	GRCh37
NC_000003.10:g.185341071C>T	NCBI36
NG_015826.1:g.10568C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.1038C>T
ENST00000468748.7:n.1258C>T
ENST00000484154.2:n.1387-1336C>T
ENST00000491008.6:n.1763C>T
ENST00000492226.2:n.1272C>T
ENST00000492773.6:c.769C>T
ENST00000647636.1:c.1015C>T	ENSP00000497505.1:p.Arg339Trp
ENST00000647909.1:c.1039C>T	ENSP00000498164.1:p.Arg347Trp
ENST00000648145.1:c.783C>T
ENST00000648189.1:c.829C>T
ENST00000648256.1:c.987C>T	ENSP00000497356.1:n.987C>T
ENST00000648314.1:c.*134C>T	ENSP00000496920.1:n.*134C>T
ENST00000648599.1:c.*298C>T	ENSP00000497159.1:n.*298C>T
ENST00000648630.1:c.1009C>T	ENSP00000497887.1:p.Arg337Trp
ENST00000648682.1:c.1015C>T	ENSP00000498185.1:p.Arg339Trp
ENST00000648882.1:c.*841C>T	ENSP00000497603.1:n.*841C>T
ENST00000648890.1:c.1015C>T	ENSP00000497503.1:p.Arg339Trp
ENST00000648915.2:c.1015C>T MANE Select	ENSP00000497160.1:p.Arg339Trp
ENST00000649545.1:c.577+432C>T
ENST00000649688.1:c.*298C>T	ENSP00000497097.1:n.*298C>T
ENST00000649814.1:n.1064C>T
ENST00000650270.1:c.882C>T
ENST00000273783.7:c.1015C>T	ENSP00000273783.3:p.Arg339Trp
ENST00000432982.5:c.246-1648C>T
ENST00000444495.1:c.1015C>T	ENSP00000409142.1:p.Arg339Trp
ENST00000479833.1:n.331C>T
ENST00000481054.5:n.1109C>T
ENST00000491144.5:n.1519C>T
ENST00000493740.1:n.245C>T
NM_003907.2:c.1015C>T	NP_003898.2:p.Arg339Trp
XM_011513265.1:c.265C>T	XP_011511567.1:p.Arg89Trp
XM_011513266.1:c.178C>T	XP_011511568.1:p.Arg60Trp
XR_924208.1:n.1966C>T
NM_003907.3:c.1015C>T MANE Select	NP_003898.2:p.Arg339Trp
XM_011513266.3:c.178C>T	XP_011511568.1:p.Arg60Trp
XR_001740352.2:n.1378C>T
XR_001740353.2:n.1378C>T
XR_924208.2:n.1378C>T