Canonical Allele Identifier: CA355381641
Gene: EIF2B5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184136710A>C , CM000665.2:g.184136710A>C GRCh38
NC_000003.11:g.183854498A>C , CM000665.1:g.183854498A>C GRCh37
NC_000003.10:g.185337192A>C NCBI36
NG_015826.1:g.6689A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000432569.2:c.294A>C ENSP00000414775.1:p.Lys98Asn
ENST00000465218.3:n.317A>C
ENST00000468748.7:n.277A>C
ENST00000471832.2:c.*288A>C ENSP00000497786.1:n.*288A>C
ENST00000484154.2:n.32A>C
ENST00000491008.6:n.159A>C
ENST00000492226.2:n.291A>C
ENST00000492773.6:c.26A>C
ENST00000647636.1:c.294A>C ENSP00000497505.1:p.Lys98Asn
ENST00000647909.1:c.294A>C ENSP00000498164.1:p.Lys98Asn
ENST00000648145.1:c.62A>C
ENST00000648189.1:c.44A>C
ENST00000648256.1:c.243A>C ENSP00000497356.1:p.Lys81Asn
ENST00000648314.1:c.294A>C ENSP00000496920.1:p.Lys98Asn
ENST00000648599.1:c.294A>C ENSP00000497159.1:p.Lys98Asn
ENST00000648630.1:c.288A>C ENSP00000497887.1:p.Lys96Asn
ENST00000648682.1:c.294A>C ENSP00000498185.1:p.Lys98Asn
ENST00000648882.1:c.*120A>C ENSP00000497603.1:n.*120A>C
ENST00000648890.1:c.294A>C ENSP00000497503.1:p.Lys98Asn
ENST00000648915.2:c.294A>C MANE Select ENSP00000497160.1:p.Lys98Asn
ENST00000649545.1:c.28A>C
ENST00000649688.1:c.294A>C ENSP00000497097.1:p.Lys98Asn
ENST00000649814.1:n.343A>C
ENST00000650244.1:c.439A>C ENSP00000497227.1:n.439A>C
ENST00000650270.1:c.161A>C
ENST00000273783.7:c.294A>C ENSP00000273783.3:p.Lys98Asn
ENST00000432569.1:c.294A>C ENSP00000414775.1:p.Lys98Asn
ENST00000432982.5:c.245+35A>C
ENST00000444495.1:c.294A>C ENSP00000409142.1:p.Lys98Asn
ENST00000471832.1:n.225A>C
ENST00000481054.5:n.295A>C
ENST00000491144.5:n.642A>C
ENST00000498831.1:n.150A>C
NM_003907.2:c.294A>C NP_003898.2:p.Lys98Asn
XR_924208.1:n.1245A>C
NM_003907.3:c.294A>C MANE Select NP_003898.2:p.Lys98Asn
XM_011513266.3:c.-608A>C XP_011511568.1:n.-608A>C
XR_001740352.2:n.657A>C
XR_001740353.2:n.657A>C
XR_924208.2:n.657A>C