Canonical Allele Identifier: CA355382362

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855799G>C (hg19) ; chr3:g.184138011G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138011G>C , CM000665.2:g.184138011G>C	GRCh38
NC_000003.11:g.183855799G>C , CM000665.1:g.183855799G>C	GRCh37
NC_000003.10:g.185338493G>C	NCBI36
NG_015826.1:g.7990G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.643G>C
ENST00000468748.7:n.603G>C
ENST00000484154.2:n.1241G>C
ENST00000491008.6:n.1368G>C
ENST00000492226.2:n.617G>C
ENST00000492773.6:c.352G>C
ENST00000647636.1:c.620G>C	ENSP00000497505.1:p.Ser207Thr
ENST00000647909.1:c.644G>C	ENSP00000498164.1:p.Ser215Thr
ENST00000648145.1:c.388G>C
ENST00000648189.1:c.370G>C
ENST00000648256.1:c.569G>C	ENSP00000497356.1:p.Ser190Thr
ENST00000648314.1:c.620G>C	ENSP00000496920.1:p.Ser207Thr
ENST00000648599.1:c.620G>C	ENSP00000497159.1:p.Ser207Thr
ENST00000648630.1:c.614G>C	ENSP00000497887.1:p.Ser205Thr
ENST00000648682.1:c.620G>C	ENSP00000498185.1:p.Ser207Thr
ENST00000648882.1:c.*446G>C	ENSP00000497603.1:n.*446G>C
ENST00000648890.1:c.620G>C	ENSP00000497503.1:p.Ser207Thr
ENST00000648915.2:c.620G>C MANE Select	ENSP00000497160.1:p.Ser207Thr
ENST00000649545.1:c.354G>C
ENST00000649688.1:c.620G>C	ENSP00000497097.1:p.Ser207Thr
ENST00000649814.1:n.669G>C
ENST00000650270.1:c.487G>C
ENST00000273783.7:c.620G>C	ENSP00000273783.3:p.Ser207Thr
ENST00000432982.5:c.245+1336G>C
ENST00000444495.1:c.620G>C	ENSP00000409142.1:p.Ser207Thr
ENST00000468748.5:n.73G>C
ENST00000481054.5:n.621G>C
ENST00000491008.5:n.584G>C
ENST00000491144.5:n.1060G>C
ENST00000498831.1:n.575G>C
NM_003907.2:c.620G>C	NP_003898.2:p.Ser207Thr
XR_924208.1:n.1571G>C
NM_003907.3:c.620G>C MANE Select	NP_003898.2:p.Ser207Thr
XM_011513266.3:c.-282G>C	XP_011511568.1:n.-282G>C
XR_001740352.2:n.983G>C
XR_001740353.2:n.983G>C
XR_924208.2:n.983G>C