Canonical Allele Identifier: CA1425881693
Gene: EIF2B5 HGNC NCBI

Linked Data

dbSNP Id: rs1713383732

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184136843G>C , CM000665.2:g.184136843G>C GRCh38
NC_000003.11:g.183854631G>C , CM000665.1:g.183854631G>C GRCh37
NC_000003.10:g.185337325G>C NCBI36
NG_015826.1:g.6822G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000432569.2:c.*103G>C ENSP00000414775.1:n.*103G>C
ENST00000465218.3:n.343+107G>C
ENST00000468748.7:n.303+107G>C
ENST00000471832.2:c.*421G>C ENSP00000497786.1:n.*421G>C
ENST00000484154.2:n.165G>C
ENST00000491008.6:n.292G>C
ENST00000492226.2:n.317+107G>C
ENST00000492773.6:c.52+107G>C
ENST00000647636.1:c.320+107G>C ENSP00000497505.1:n.320+107G>C
ENST00000647909.1:c.320+107G>C ENSP00000498164.1:n.320+107G>C
ENST00000648145.1:c.88+107G>C
ENST00000648189.1:c.70+107G>C
ENST00000648256.1:c.269+107G>C ENSP00000497356.1:n.269+107G>C
ENST00000648314.1:c.320+107G>C ENSP00000496920.1:n.320+107G>C
ENST00000648599.1:c.320+107G>C ENSP00000497159.1:n.320+107G>C
ENST00000648630.1:c.314+107G>C ENSP00000497887.1:n.314+107G>C
ENST00000648682.1:c.320+107G>C ENSP00000498185.1:n.320+107G>C
ENST00000648882.1:c.*146+107G>C ENSP00000497603.1:n.*146+107G>C
ENST00000648890.1:c.320+107G>C ENSP00000497503.1:n.320+107G>C
ENST00000648915.2:c.320+107G>C MANE Select ENSP00000497160.1:n.320+107G>C
ENST00000649545.1:c.54+107G>C
ENST00000649688.1:c.320+107G>C ENSP00000497097.1:n.320+107G>C
ENST00000649814.1:n.369+107G>C
ENST00000650244.1:c.465+107G>C ENSP00000497227.1:n.465+107G>C
ENST00000650270.1:c.187+107G>C
ENST00000273783.7:c.320+107G>C ENSP00000273783.3:n.320+107G>C
ENST00000432569.1:c.*103G>C ENSP00000414775.1:n.*103G>C
ENST00000432982.5:c.245+168G>C
ENST00000444495.1:c.320+107G>C ENSP00000409142.1:n.320+107G>C
ENST00000471832.1:n.358G>C
ENST00000481054.5:n.321+107G>C
ENST00000491144.5:n.668+107G>C
ENST00000498831.1:n.176+107G>C
NM_003907.2:c.320+107G>C NP_003898.2:n.320+107G>C
XR_924208.1:n.1271+107G>C
NM_003907.3:c.320+107G>C MANE Select NP_003898.2:n.320+107G>C
XM_011513266.3:c.-582+107G>C XP_011511568.1:n.-582+107G>C
XR_001740352.2:n.683+107G>C
XR_001740353.2:n.683+107G>C
XR_924208.2:n.683+107G>C