Canonical Allele Identifier: CA355382400

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855817T>C (hg19) ; chr3:g.184138029T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138029T>C , CM000665.2:g.184138029T>C	GRCh38
NC_000003.11:g.183855817T>C , CM000665.1:g.183855817T>C	GRCh37
NC_000003.10:g.185338511T>C	NCBI36
NG_015826.1:g.8008T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.661T>C
ENST00000468748.7:n.621T>C
ENST00000484154.2:n.1259T>C
ENST00000491008.6:n.1386T>C
ENST00000492226.2:n.635T>C
ENST00000492773.6:c.370T>C
ENST00000647636.1:c.638T>C	ENSP00000497505.1:p.Leu213Pro
ENST00000647909.1:c.662T>C	ENSP00000498164.1:p.Leu221Pro
ENST00000648145.1:c.406T>C
ENST00000648189.1:c.388T>C
ENST00000648256.1:c.587T>C	ENSP00000497356.1:p.Leu196Pro
ENST00000648314.1:c.638T>C	ENSP00000496920.1:p.Leu213Pro
ENST00000648599.1:c.638T>C	ENSP00000497159.1:p.Leu213Pro
ENST00000648630.1:c.632T>C	ENSP00000497887.1:p.Leu211Pro
ENST00000648682.1:c.638T>C	ENSP00000498185.1:p.Leu213Pro
ENST00000648882.1:c.*464T>C	ENSP00000497603.1:n.*464T>C
ENST00000648890.1:c.638T>C	ENSP00000497503.1:p.Leu213Pro
ENST00000648915.2:c.638T>C MANE Select	ENSP00000497160.1:p.Leu213Pro
ENST00000649545.1:c.372T>C
ENST00000649688.1:c.638T>C	ENSP00000497097.1:p.Leu213Pro
ENST00000649814.1:n.687T>C
ENST00000650270.1:c.505T>C
ENST00000273783.7:c.638T>C	ENSP00000273783.3:p.Leu213Pro
ENST00000432982.5:c.245+1354T>C
ENST00000444495.1:c.638T>C	ENSP00000409142.1:p.Leu213Pro
ENST00000468748.5:n.91T>C
ENST00000481054.5:n.639T>C
ENST00000491008.5:n.602T>C
ENST00000491144.5:n.1078T>C
ENST00000498831.1:n.593T>C
NM_003907.2:c.638T>C	NP_003898.2:p.Leu213Pro
XR_924208.1:n.1589T>C
NM_003907.3:c.638T>C MANE Select	NP_003898.2:p.Leu213Pro
XM_011513266.3:c.-264T>C	XP_011511568.1:n.-264T>C
XR_001740352.2:n.1001T>C
XR_001740353.2:n.1001T>C
XR_924208.2:n.1001T>C