Canonical Allele Identifier: CA355384670

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183858227A>C (hg19) ; chr3:g.184140439A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184140439A>C , CM000665.2:g.184140439A>C	GRCh38
NC_000003.11:g.183858227A>C , CM000665.1:g.183858227A>C	GRCh37
NC_000003.10:g.185340921A>C	NCBI36
NG_015826.1:g.10418A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.888A>C
ENST00000468748.7:n.1108A>C
ENST00000484154.2:n.1387-1486A>C
ENST00000491008.6:n.1613A>C
ENST00000492226.2:n.1122A>C
ENST00000492773.6:c.619A>C
ENST00000647636.1:c.865A>C	ENSP00000497505.1:p.Met289Leu
ENST00000647909.1:c.889A>C	ENSP00000498164.1:p.Met297Leu
ENST00000648145.1:c.633A>C
ENST00000648189.1:c.679A>C
ENST00000648256.1:c.837A>C	ENSP00000497356.1:n.837A>C
ENST00000648314.1:c.929A>C	ENSP00000496920.1:p.His310Pro
ENST00000648599.1:c.*148A>C	ENSP00000497159.1:n.*148A>C
ENST00000648630.1:c.859A>C	ENSP00000497887.1:p.Met287Leu
ENST00000648682.1:c.865A>C	ENSP00000498185.1:p.Met289Leu
ENST00000648882.1:c.*691A>C	ENSP00000497603.1:n.*691A>C
ENST00000648890.1:c.865A>C	ENSP00000497503.1:p.Met289Leu
ENST00000648915.2:c.865A>C MANE Select	ENSP00000497160.1:p.Met289Leu
ENST00000649545.1:c.577+282A>C
ENST00000649688.1:c.*148A>C	ENSP00000497097.1:n.*148A>C
ENST00000649814.1:n.914A>C
ENST00000650270.1:c.732A>C
ENST00000273783.7:c.865A>C	ENSP00000273783.3:p.Met289Leu
ENST00000432982.5:c.246-1798A>C
ENST00000444495.1:c.865A>C	ENSP00000409142.1:p.Met289Leu
ENST00000468748.5:n.578A>C
ENST00000479833.1:n.181A>C
ENST00000481054.5:n.959A>C
ENST00000491144.5:n.1369A>C
ENST00000493740.1:n.95A>C
NM_003907.2:c.865A>C	NP_003898.2:p.Met289Leu
XM_011513265.1:c.115A>C	XP_011511567.1:p.Met39Leu
XM_011513266.1:c.28A>C	XP_011511568.1:p.Met10Leu
XR_924208.1:n.1816A>C
NM_003907.3:c.865A>C MANE Select	NP_003898.2:p.Met289Leu
XM_011513266.3:c.28A>C	XP_011511568.1:p.Met10Leu
XR_001740352.2:n.1228A>C
XR_001740353.2:n.1228A>C
XR_924208.2:n.1228A>C